ID stringlengths 13 17 | question stringlengths 88 1.13k | answer stringlengths 6 156 | reference_sequence stringlengths 4.1k 4.1k | variant_sequence stringlengths 4.1k 4.1k |
|---|---|---|---|---|
Task1_train_42100 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | GATTTCTGTCGTGATTCACTGGGGCCGCTAACGTGCACTCCCTCTTTTCATCTTAGGACATGACACCAGTGGCATATCACGGCCATGGGGTCTCAGCATTCCGCTGCTGCTCGCCCCTCCTCCTGCAGGCGAAAGCAAGAAGATGACAGGGACGGTTTGCTGGCTGAACGAGAGCAGGAAGAAGCCATTGCTCAGTTCCCATATGTGGAATTCACCGGGAGAGATAGCATCACCTGTCTCACGTGCCAGGGGACAGGCTACATTCCAACAGGTGATCATGGAGGGATGATTCCCTGATGAGAATCCCAAGGTACCCTCGG... | GATTTCTGTCGTGATTCACTGGGGCCGCTAACGTGCACTCCCTCTTTTCATCTTAGGACATGACACCAGTGGCATATCACGGCCATGGGGTCTCAGCATTCCGCTGCTGCTCGCCCCTCCTCCTGCAGGCGAAAGCAAGAAGATGACAGGGACGGTTTGCTGGCTGAACGAGAGCAGGAAGAAGCCATTGCTCAGTTCCCATATGTGGAATTCACCGGGAGAGATAGCATCACCTGTCTCACGTGCCAGGGGACAGGCTACATTCCAACAGGTGATCATGGAGGGATGATTCCCTGATGAGAATCCCAAGGTACCCTCGG... |
Task1_train_42101 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | GCTCTCTGTTTTATCAGTTGTGCCAAATATTTGGAAATTTACTTCACAGAATGCTACTGCCCTCTGATTGATTTGGAGTCTCCCGCCCACTTCCCGCGTTCCCGTCACCGTGGAGAAGGGGACAACTTGCTCATTGTTGCCACCTGTCCAGGTCATTGAAAGGCAAGGGACACCCAAGAGTAGGAAGAAATGGGAAGCAGTCCATTCTTAAGCCTGGTGTTCAGAGTCCGTGGAAATTTTAAGTGCAGGCCCAGGGAGTGAAGAATGGGGGCCACAGTGGCGGGGGCAGGAGGAATATGGGTGGGCCAGGTCACATTTCC... | GCTCTCTGTTTTATCAGTTGTGCCAAATATTTGGAAATTTACTTCACAGAATGCTACTGCCCTCTGATTGATTTGGAGTCTCCCGCCCACTTCCCGCGTTCCCGTCACCGTGGAGAAGGGGACAACTTGCTCATTGTTGCCACCTGTCCAGGTCATTGAAAGGCAAGGGACACCCAAGAGTAGGAAGAAATGGGAAGCAGTCCATTCTTAAGCCTGGTGTTCAGAGTCCGTGGAAATTTTAAGTGCAGGCCCAGGGAGTGAAGAATGGGGGCCACAGTGGCGGGGGCAGGAGGAATATGGGTGGGCCAGGTCACATTTCC... |
Task1_train_42102 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | CCTCCCTCTAGCATACCTCCCTTCTCAAGTTTTGGTTTCTGGTCCTGTTCAACAGTGGGTTCCACATAGTGCCAAGGTTTACCAGAGAGGCAAGTTCATGTTTGTGTGAGGCTGCTAACCCTGGCGGTGTGGCTTCAGTGTCCTTACTCTCGGTTGAAAAATCAACAGAAGAAGTCCTTAGGACTGCTATTTGGGCATGCCTACAGAACGGAGGATTAATGGAAAACAAACTAAAGAACAAACCACAAGTCAATATGTACTTTCCAATAATCTTTTCATTTTTAATATCAATTGATGTTTTAAAAAATACAGAGGTGTTT... | CCTCCCTCTAGCATACCTCCCTTCTCAAGTTTTGGTTTCTGGTCCTGTTCAACAGTGGGTTCCACATAGTGCCAAGGTTTACCAGAGAGGCAAGTTCATGTTTGTGTGAGGCTGCTAACCCTGGCGGTGTGGCTTCAGTGTCCTTACTCTCGGTTGAAAAATCAACAGAAGAAGTCCTTAGGACTGCTATTTGGGCATGCCTACAGAACGGAGGATTAATGGAAAACAAACTAAAGAACAAACCACAAGTCAATATGTACTTTCCAATAATCTTTTCATTTTTAATATCAATTGATGTTTTAAAAAATACAGAGGTGTTT... |
Task1_train_42103 | An alteration has been detected on Chromosome 12. Is it pathogenic, and if so, what disease is involved? | Benign | GGAGGCGAGGGCTCTGAAATGCAGATGAGGGTCAAAGACGCCGCCGCCAGTAAGTTTCTCAAACTCGTGGAAAGATGGAGAGGAGGGGTGTGGCCGAGCTCTAGGTGTCTGACATTCCTGACGTCCACGCAGACTGCGCATTTCCCCACGTCACACCTTTGGGTCCGCTGACCCCAGGCGGGGGAAGTTATAAAAGGTGGGATGCTCCAGGGCGCAAAATCAGCCTCTCGGATGCAGAATCACACTCCCTCTGGGAGGAGGAGCGACTGGAAGGTTTGGGCCGGAGAAGCTGTGGAATCACTCCCTCCCAGGAAAGATGC... | GGAGGCGAGGGCTCTGAAATGCAGATGAGGGTCAAAGACGCCGCCGCCAGTAAGTTTCTCAAACTCGTGGAAAGATGGAGAGGAGGGGTGTGGCCGAGCTCTAGGTGTCTGACATTCCTGACGTCCACGCAGACTGCGCATTTCCCCACGTCACACCTTTGGGTCCGCTGACCCCAGGCGGGGGAAGTTATAAAAGGTGGGATGCTCCAGGGCGCAAAATCAGCCTCTCGGATGCAGAATCACACTCCCTCTGGGAGGAGGAGCGACTGGAAGGTTTGGGCCGGAGAAGCTGTGGAATCACTCCCTCCCAGGAAAGATGC... |
Task1_train_42104 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | ATGAGCGCTAGGGCTGCACCTTGCTCCAGGGCCAGCTGGGAGGGGGAGGGTACCCTAAAGAGGCGCTGAGGTCTCAGAGGGCCTATCGGAAGCCGTTCTTTGTGGCCTGGGATTTCAGCCCACCAGTGTCAGAGTGTTAGTCCCCTTTGTCTAACTCTGCTTTGAGCCCACCAGCCACCAAGCCTTGGACAGGCTGTGAAGTCAACCCTTTGGCGTTTGCTTGCTCCCTCGCTCGCGCTCTCTCTTTCCTACTTCACCTAAGTTCGATGAGTTGAGATCTGTTTTTGCTGAACTCGAAGTGCTTCGAAGAGGCGAGCTGT... | ATGAGCGCTAGGGCTGCACCTTGCTCCAGGGCCAGCTGGGAGGGGGAGGGTACCCTAAAGAGGCGCTGAGGTCTCAGAGGGCCTATCGGAAGCCGTTCTTTGTGGCCTGGGATTTCAGCCCACCAGTGTCAGAGTGTTAGTCCCCTTTGTCTAACTCTGCTTTGAGCCCACCAGCCACCAAGCCTTGGACAGGCTGTGAAGTCAACCCTTTGGCGTTTGCTTGCTCCCTCGCTCGCGCTCTCTCTTTCCTACTTCACCTAAGTTCGATGAGTTGAGATCTGTTTTTGCTGAACTCGAAGTGCTTCGAAGAGGCGAGCTGT... |
Task1_train_42105 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | AAAGAGAAACGAGGCATAGATCCAGAGATCACGTTAGGGTACACCAAGAAAGAGACGGTTCAAGGGAATTACCAGGAGGCGATGAGCCAGGTAAGCAAATTGTGGCAGTTAAGGGGATTTTCATAACCTGAGCAGGAGGGTCCAGACGTTTCTTTCTGATGGTGGCACTAGCGATATCACATCTCAGGGAGATACCACAGAGTAGGAGAGTTGGAGAAATGTTTACGTGAGACGCAGAAGTAGTCAAGAAATATCACTCGGGTCTCAAGGAAGGCGGGAGATGAAGCCGGTACCACAGAAAGCCGAGCTTCCCGGTGAAA... | AAAGAGAAACGAGGCATAGATCCAGAGATCACGTTAGGGTACACCAAGAAAGAGACGGTTCAAGGGAATTACCAGGAGGCGATGAGCCAGGTAAGCAAATTGTGGCAGTTAAGGGGATTTTCATAACCTGAGCAGGAGGGTCCAGACGTTTCTTTCTGATGGTGGCACTAGCGATATCACATCTCAGGGAGATACCACAGAGTAGGAGAGTTGGAGAAATGTTTACGTGAGACGCAGAAGTAGTCAAGAAATATCACTCGGGTCTCAAGGAAGGCGGGAGATGAAGCCGGTACCACAGAAAGCCGAGCTTCCCGGTGAAA... |
Task1_train_42106 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | CTGTCTATTCAAGCCTTTGCTCATTTTTAAATTTTTTATGTTTGAGACAGGATCTCACTCTGTCGCCCAGGGTGGAGTGTGGTGGCGCAATCTCGGCTCACTGCAAGCTCTGCCTCCCAGGCTCAAGTCATTCTTGTGCCTCAACCTCCTGAGTAGCTGGGACTACAGGCATGTGCCACCACACCTGGCTAATTTTTTGTATTTTTGTAGAGACGGGGTTTCACCATGTTGCCCAGTCTGGTCTTAAATTCCGGAGCTCAAACAATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATTGTGCC... | CTGTCTATTCAAGCCTTTGCTCATTTTTAAATTTTTTATGTTTGAGACAGGATCTCACTCTGTCGCCCAGGGTGGAGTGTGGTGGCGCAATCTCGGCTCACTGCAAGCTCTGCCTCCCAGGCTCAAGTCATTCTTGTGCCTCAACCTCCTGAGTAGCTGGGACTACAGGCATGTGCCACCACACCTGGCTAATTTTTTGTATTTTTGTAGAGACGGGGTTTCACCATGTTGCCCAGTCTGGTCTTAAATTCCGGAGCTCAAACAATCCACCTGCCTTGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCATTGTGCC... |
Task1_train_42107 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | TTTTATAAGGTCCACCTGCTTTCTTGTATCAGATTTTATAATCTTTTAGAGCAAGTCGCGTTTCTTTCCTTCCCTCCCACCAACTTCCCCTTCTCCTTTTCTCCATGGTTATCAAGACCATCTGTTATCATTGGCCCCCTAGGAAGCAGGTTGGAGGAGATAGGATGAGCCAAAAATAAGAATTAAGATTAACTATTAGGAAGGATATCCACATCCCAGTATTTCAAAAATGGGAGAAAGTAGAAGAGAGTATTGCAAAAGTTGATGCCTCCTTCTTTGGACTGTGTTAAATATGATAGTCTCACGAGCATCCAGGACTC... | TTTTATAAGGTCCACCTGCTTTCTTGTATCAGATTTTATAATCTTTTAGAGCAAGTCGCGTTTCTTTCCTTCCCTCCCACCAACTTCCCCTTCTCCTTTTCTCCATGGTTATCAAGACCATCTGTTATCATTGGCCCCCTAGGAAGCAGGTTGGAGGAGATAGGATGAGCCAAAAATAAGAATTAAGATTAACTATTAGGAAGGATATCCACATCCCAGTATTTCAAAAATGGGAGAAAGTAGAAGAGAGTATTGCAAAAGTTGATGCCTCCTTCTTTGGACTGTGTTAAATATGATAGTCTCACGAGCATCCAGGACTC... |
Task1_train_42108 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | AATAGGGAAAGGGCTTGTCACAAAGGTTGGGGATACTCAGTGTATGTCTGAACTTGGGCACTGAAAGAGAGAGCGGGAATTACTCTAACACACAGTCCCCCCATCCATACCCTCCACACAACGGTCAACAGTTTACCTTTTCACCTGTGAGATGATGCAGACTGTTATTCAGAATTAGAAATAGTATTATAGATTATCCAGTCCAATTCCCTAACAGATGAGGAAAATGATGTGGCCAAGGTCGCTGAATGAATAAGTGGCAGAAACGAAACTGAATTCAGGTCTCCTAAAACCCACTACGTTTGGCTTGGGGAGTTCTG... | AATAGGGAAAGGGCTTGTCACAAAGGTTGGGGATACTCAGTGTATGTCTGAACTTGGGCACTGAAAGAGAGAGCGGGAATTACTCTAACACACAGTCCCCCCATCCATACCCTCCACACAACGGTCAACAGTTTACCTTTTCACCTGTGAGATGATGCAGACTGTTATTCAGAATTAGAAATAGTATTATAGATTATCCAGTCCAATTCCCTAACAGATGAGGAAAATGATGTGGCCAAGGTCGCTGAATGAATAAGTGGCAGAAACGAAACTGAATTCAGGTCTCCTAAAACCCACTACGTTTGGCTTGGGGAGTTCTG... |
Task1_train_42109 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTTGTTTTGTTTTGTTTTGCCTGAGATAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGTAATTATGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGTGATCCTCCTGCCTCAGCCTCTCAAGTAGCTAGAATTACAAGCATGCGCTACCACGCCCAGCTAATTTTTGTATTTTTATTAGAGACGGGGTTTCACCATGTTGACCAAGCTGGTCTTGAGCTCCTGGCCTCAAGTAATCTGCCCACCTTGGCCTCCCACAGTGCTGGAATCACAGGTGTGAGCCACCACGTGCTGCCAGAAGCTACTGTTTTA... | TTTGTTTTGTTTTGTTTTGCCTGAGATAGAGTCTCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGTAATTATGGCTCACTGCAGCCTCTGCCTCCTGGGTTCAAGTGATCCTCCTGCCTCAGCCTCTCAAGTAGCTAGAATTACAAGCATGCGCTACCACGCCCAGCTAATTTTTGTATTTTTATTAGAGACGGGGTTTCACCATGTTGACCAAGCTGGTCTTGAGCTCCTGGCCTCAAGTAATCTGCCCACCTTGGCCTCCCACAGTGCTGGAATCACAGGTGTGAGCCACCACGTGCTGCCAGAAGCTACTGTTTTA... |
Task1_train_42110 | A change on Chromosome 12 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | ATCTGCCCACCTTGGCCTCCCACAGTGCTGGAATCACAGGTGTGAGCCACCACGTGCTGCCAGAAGCTACTGTTTTAAGTCATCATTGCAAAGGGTAGTGTGTGATGCGCAGGAGTGGAAAGGGCAGTACATCTATTTGAGAGCATCCCAAATGAGGTCCATTCATATTATGGAAGTGCACTGCGAAATAAAGAACAGGCCTACCCCCTTGTTTTATTATGAAGGGGTATGAGAAAAATGCAATTTTCAAAGAAAGAGAACTGCTGAGGATGTAGTACCTTCTCAAAGAAAGCTGTGTTTGGTTAAGGTGAGAAGCTAGA... | ATCTGCCCACCTTGGCCTCCCACAGTGCTGGAATCACAGGTGTGAGCCACCACGTGCTGCCAGAAGCTACTGTTTTAAGTCATCATTGCAAAGGGTAGTGTGTGATGCGCAGGAGTGGAAAGGGCAGTACATCTATTTGAGAGCATCCCAAATGAGGTCCATTCATATTATGGAAGTGCACTGCGAAATAAAGAACAGGCCTACCCCCTTGTTTTATTATGAAGGGGTATGAGAAAAATGCAATTTTCAAAGAAAGAGAACTGCTGAGGATGTAGTACCTTCTCAAAGAAAGCTGTGTTTGGTTAAGGTGAGAAGCTAGA... |
Task1_train_42111 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | GAAGCTACTGTTTTAAGTCATCATTGCAAAGGGTAGTGTGTGATGCGCAGGAGTGGAAAGGGCAGTACATCTATTTGAGAGCATCCCAAATGAGGTCCATTCATATTATGGAAGTGCACTGCGAAATAAAGAACAGGCCTACCCCCTTGTTTTATTATGAAGGGGTATGAGAAAAATGCAATTTTCAAAGAAAGAGAACTGCTGAGGATGTAGTACCTTCTCAAAGAAAGCTGTGTTTGGTTAAGGTGAGAAGCTAGAGGAAGCCACAGAGGGCAGGGTTACAAATTGAAAGACTTCTGCAATGGTAGAGGTAGTATGCA... | GAAGCTACTGTTTTAAGTCATCATTGCAAAGGGTAGTGTGTGATGCGCAGGAGTGGAAAGGGCAGTACATCTATTTGAGAGCATCCCAAATGAGGTCCATTCATATTATGGAAGTGCACTGCGAAATAAAGAACAGGCCTACCCCCTTGTTTTATTATGAAGGGGTATGAGAAAAATGCAATTTTCAAAGAAAGAGAACTGCTGAGGATGTAGTACCTTCTCAAAGAAAGCTGTGTTTGGTTAAGGTGAGAAGCTAGAGGAAGCCACAGAGGGCAGGGTTACAAATTGAAAGACTTCTGCAATGGTAGAGGTAGTATGCA... |
Task1_train_42112 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | TAGTGTGTGATGCGCAGGAGTGGAAAGGGCAGTACATCTATTTGAGAGCATCCCAAATGAGGTCCATTCATATTATGGAAGTGCACTGCGAAATAAAGAACAGGCCTACCCCCTTGTTTTATTATGAAGGGGTATGAGAAAAATGCAATTTTCAAAGAAAGAGAACTGCTGAGGATGTAGTACCTTCTCAAAGAAAGCTGTGTTTGGTTAAGGTGAGAAGCTAGAGGAAGCCACAGAGGGCAGGGTTACAAATTGAAAGACTTCTGCAATGGTAGAGGTAGTATGCAGAAGGGTTCCTTAAAATACAGGGATCCATGTAA... | TAGTGTGTGATGCGCAGGAGTGGAAAGGGCAGTACATCTATTTGAGAGCATCCCAAATGAGGTCCATTCATATTATGGAAGTGCACTGCGAAATAAAGAACAGGCCTACCCCCTTGTTTTATTATGAAGGGGTATGAGAAAAATGCAATTTTCAAAGAAAGAGAACTGCTGAGGATGTAGTACCTTCTCAAAGAAAGCTGTGTTTGGTTAAGGTGAGAAGCTAGAGGAAGCCACAGAGGGCAGGGTTACAAATTGAAAGACTTCTGCAATGGTAGAGGTAGTATGCAGAAGGGTTCCTTAAAATACAGGGATCCATGTAA... |
Task1_train_42113 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTTTGTCTCAAAAAAAAAAAAAAAAAATTAGCTGGATGTGGTGGCACATGCTTGTAATCCCAGCTTCTTGGGAGGGTGAGACACAGGAATTGCTTGAACCCAGGAGGTGGAGGTTACAGTGAGCCAAGATTGTGCCATTACATAGCCTGGGCTGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAGCACTGGTCTAAGCTACTTCCTGGAGCTTTGATTTTTAAAAGAAACTGTCACTGTCTAGCCTGTGACTGATGAATGTATGTGATTGCCCTCTGGAAAAGT... | CCACTGCACTCCAGCCTGGGCAACAGAGTGAGACTTTGTCTCAAAAAAAAAAAAAAAAAATTAGCTGGATGTGGTGGCACATGCTTGTAATCCCAGCTTCTTGGGAGGGTGAGACACAGGAATTGCTTGAACCCAGGAGGTGGAGGTTACAGTGAGCCAAGATTGTGCCATTACATAGCCTGGGCTGAGCAAGACTCTGTCTCAAAAAAAAAAAAAAAAAGCACTGGTCTAAGCTACTTCCTGGAGCTTTGATTTTTAAAAGAAACTGTCACTGTCTAGCCTGTGACTGATGAATGTATGTGATTGCCCTCTGGAAAAGT... |
Task1_train_42114 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | CTGTCTAGCCTGTGACTGATGAATGTATGTGATTGCCCTCTGGAAAAGTATGATATGCTTGGCAATTTGAAGTATTCTTAGAATAATACTTTAAATTATTCCCAACTAAACTGTGTCCAAAATAGGTCCTTGATAAGCTAATCCTTACTTGGCCCCCTTCATTTCCAACCCTTTGAAATTCACTCTGCTCCTTTCTCCTGATCTTCTGGAAGTTTCTTTCTGAATCTAGAGAAACTCTCCTCACCAGAGAGGAATGATGTAAGCAGGCTCAATTAAATGCCCGCTGTGTATAATGAAGCATATTGTTAGGTGCAGCATGG... | CTGTCTAGCCTGTGACTGATGAATGTATGTGATTGCCCTCTGGAAAAGTATGATATGCTTGGCAATTTGAAGTATTCTTAGAATAATACTTTAAATTATTCCCAACTAAACTGTGTCCAAAATAGGTCCTTGATAAGCTAATCCTTACTTGGCCCCCTTCATTTCCAACCCTTTGAAATTCACTCTGCTCCTTTCTCCTGATCTTCTGGAAGTTTCTTTCTGAATCTAGAGAAACTCTCCTCACCAGAGAGGAATGATGTAAGCAGGCTCAATTAAATGCCCGCTGTGTATAATGAAGCATATTGTTAGGTGCAGCATGG... |
Task1_train_42115 | An alteration has been detected on Chromosome 12. Is it pathogenic, and if so, what disease is involved? | Benign | CCTTTCTCCTGATCTTCTGGAAGTTTCTTTCTGAATCTAGAGAAACTCTCCTCACCAGAGAGGAATGATGTAAGCAGGCTCAATTAAATGCCCGCTGTGTATAATGAAGCATATTGTTAGGTGCAGCATGGGACATAGAAGTTCAAAGACTATAGCTCTTGAGGATATCTTTATTTAGTTGGAAATACAAGACAGAAACATTCAAAGTAAAGTAAATTTATTCCTTATATTTAGGTAGCCCTTGTTCATCTACCTCTTCTGAAATTTTGCAATAATTCTGTGATGTTGGTAGGAAGGGAATGTGATGTTAGATAAGAAGT... | CCTTTCTCCTGATCTTCTGGAAGTTTCTTTCTGAATCTAGAGAAACTCTCCTCACCAGAGAGGAATGATGTAAGCAGGCTCAATTAAATGCCCGCTGTGTATAATGAAGCATATTGTTAGGTGCAGCATGGGACATAGAAGTTCAAAGACTATAGCTCTTGAGGATATCTTTATTTAGTTGGAAATACAAGACAGAAACATTCAAAGTAAAGTAAATTTATTCCTTATATTTAGGTAGCCCTTGTTCATCTACCTCTTCTGAAATTTTGCAATAATTCTGTGATGTTGGTAGGAAGGGAATGTGATGTTAGATAAGAAGT... |
Task1_train_42116 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | TGGGTTTCGCTAAGGTGCTTGGGTAATAACCAAGATGGAATCACTATGGTGCAACACCCCTGGGGGAACTTTACCCCTCCCATTATGACAGAACCCACAGAAGACTTCTTTTGCCACATAAAAAACCCAGAACTCAGCCTCATTTCTGACAACCCACTTTTGAGTCCCCTCTTGCTGCTAAGAGCTTTTCTGTTGCTTAGTAAATTCTACTCTGCCTTACTTACTCTCTGGTGTCTGCTTGCCTTCTTCTTGGTCATGGGACAAGAACTCAGACCTCGCTAAACAAAGGAGTTAAGAAGGCTGCAATACTAGGTGGTCTA... | TGGGTTTCGCTAAGGTGCTTGGGTAATAACCAAGATGGAATCACTATGGTGCAACACCCCTGGGGGAACTTTACCCCTCCCATTATGACAGAACCCACAGAAGACTTCTTTTGCCACATAAAAAACCCAGAACTCAGCCTCATTTCTGACAACCCACTTTTGAGTCCCCTCTTGCTGCTAAGAGCTTTTCTGTTGCTTAGTAAATTCTACTCTGCCTTACTTACTCTCTGGTGTCTGCTTGCCTTCTTCTTGGTCATGGGACAAGAACTCAGACCTCGCTAAACAAAGGAGTTAAGAAGGCTGCAATACTAGGTGGTCTA... |
Task1_train_42117 | Mutation context: Chromosome 12. Determine if this variant is likely to be benign or pathogenic. Mention the disease if applicable. | Benign | CAAGGGCATTTCCTAGGTTTTCTTCTAGAATTTGTTTTCAATTTTTATGTTTATTTATTCTTTTTTAATTTTTTAAAATTTTGTGGGTGCATATTAGATATATATACTTATGGCGTACATGGGATGTTTTGATACAGGCATGCAATGTGAAATAAGCACATCATGGATAATGGAGTATCCATCCCCAGAAGCATTTATCTTTCAAGTTACAAATAATGCAATTACACTCTTTAAATTATTTTTAAATGTACAATTAAGTTATTTTTATTATAGTCACCCTGTTGTGCTATCAAATAGTAGGTCTTATTCATTCTTTTTAT... | CAAGGGCATTTCCTAGGTTTTCTTCTAGAATTTGTTTTCAATTTTTATGTTTATTTATTCTTTTTTAATTTTTTAAAATTTTGTGGGTGCATATTAGATATATATACTTATGGCGTACATGGGATGTTTTGATACAGGCATGCAATGTGAAATAAGCACATCATGGATAATGGAGTATCCATCCCCAGAAGCATTTATCTTTCAAGTTACAAATAATGCAATTACACTCTTTAAATTATTTTTAAATGTACAATTAAGTTATTTTTATTATAGTCACCCTGTTGTGCTATCAAATAGTAGGTCTTATTCATTCTTTTTAT... |
Task1_train_42118 | A variant has been detected on Chromosome 12. What is its effect — pathogenic or benign? If pathogenic, name the disease. | Benign | ATTTACTTGGAGTTTCTAAGAGGTCTTCACATAAATACCAGCTACTTCAACATCCCAATCTTACCATATTAGTTGCTTGTAAAACCTTAGATAGAGATGAGAATTAAAAGATAATTGATCACTTTTGAACTTATAGGAAACTGAGCAGGAAAAGACTGTTAATTAAGTCAATGGCTATGGCTTTCTGATTAAAATGAGTAAAATTCTCCAGAGCCTCTTGTGCCAGCCCCCACTGTACAATATTATTTAAAATGAATAATGTGTCCAACATGCTTTATTTTCTGTGACATTCAATGACTCTTTACATAAGGAAATAATCT... | ATTTACTTGGAGTTTCTAAGAGGTCTTCACATAAATACCAGCTACTTCAACATCCCAATCTTACCATATTAGTTGCTTGTAAAACCTTAGATAGAGATGAGAATTAAAAGATAATTGATCACTTTTGAACTTATAGGAAACTGAGCAGGAAAAGACTGTTAATTAAGTCAATGGCTATGGCTTTCTGATTAAAATGAGTAAAATTCTCCAGAGCCTCTTGTGCCAGCCCCCACTGTACAATATTATTTAAAATGAATAATGTGTCCAACATGCTTTATTTTCTGTGACATTCAATGACTCTTTACATAAGGAAATAATCT... |
Task1_train_42119 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | GGCCAGATTTCTGGTGCCACATTCTGCAACTGCCTCTCTGATGGGCCTGTTAGGTGGTCAGTGTCCCTTCAAGTCTGGACCCTCCCACTTTGACTATACTTCAAATCAAGGATGTGAGCTGGGCAGCTGGGGAGACATGTCCAGGCCCCTGTAACAGAATGACTCTTCTCTGTGTCCACTTTAGGGATGAGCAACTGCTCCATGACACCCATGACATCAGCACCCAGGACTGGGTAAGTGTCCCTATTCTGACAATGTTCAAGGGAGATGGCACCCACCTGGATATGGGTGTGCTGGCCATGAATATAGCTAGCTCTGAG... | GGCCAGATTTCTGGTGCCACATTCTGCAACTGCCTCTCTGATGGGCCTGTTAGGTGGTCAGTGTCCCTTCAAGTCTGGACCCTCCCACTTTGACTATACTTCAAATCAAGGATGTGAGCTGGGCAGCTGGGGAGACATGTCCAGGCCCCTGTAACAGAATGACTCTTCTCTGTGTCCACTTTAGGGATGAGCAACTGCTCCATGACACCCATGACATCAGCACCCAGGACTGGGTAAGTGTCCCTATTCTGACAATGTTCAAGGGAGATGGCACCCACCTGGATATGGGTGTGCTGGCCATGAATATAGCTAGCTCTGAG... |
Task1_train_42120 | A genomic variant on Chromosome 12 is under review. What is the biological outcome — benign or pathogenic? | Benign | CACTGTTGTAACCCAGACCTGAAGACTCATGAAATACATACTTGAGGGCCATGAGGGAGAACACATTCTGGCCATAAGGGAGAAATCTGGCCATAAGGGAGAAATGATCAGAGAATAGTGGGACAGGACATCCCCCTGTAAGGTAGGGATTACCAGCAGCAGGCATTTCCAGCAGAAACTAGATGCTCAGAGTCCAACTTTGCAGTCCTACAAGATGAATTCCCAACTTTTTTCCTATTGTCTGAGACAGTGGTCCAGAATCTGCAGTACTGCACAGAATCCTGGCTGTTGCTACACCCTATATACCCACTCATGTATTC... | CACTGTTGTAACCCAGACCTGAAGACTCATGAAATACATACTTGAGGGCCATGAGGGAGAACACATTCTGGCCATAAGGGAGAAATCTGGCCATAAGGGAGAAATGATCAGAGAATAGTGGGACAGGACATCCCCCTGTAAGGTAGGGATTACCAGCAGCAGGCATTTCCAGCAGAAACTAGATGCTCAGAGTCCAACTTTGCAGTCCTACAAGATGAATTCCCAACTTTTTTCCTATTGTCTGAGACAGTGGTCCAGAATCTGCAGTACTGCACAGAATCCTGGCTGTTGCTACACCCTATATACCCACTCATGTATTC... |
Task1_train_42121 | A mutation has occurred on Chromosome 12. What is the medical relevance of this mutation? | Benign | CCTGTAAGGTAGGGATTACCAGCAGCAGGCATTTCCAGCAGAAACTAGATGCTCAGAGTCCAACTTTGCAGTCCTACAAGATGAATTCCCAACTTTTTTCCTATTGTCTGAGACAGTGGTCCAGAATCTGCAGTACTGCACAGAATCCTGGCTGTTGCTACACCCTATATACCCACTCATGTATTCCTGTATCATGAAATCCTTTCAAGTCTTCCTCTTGCTTACTTGTCCAGAGATTCCAGGCATTCCTGGGATACACATCTTCCCTAGTAATTATATCGAAGATTCCCCTAGGTGTCTACATGAGTCCCAACCAACTT... | CCTGTAAGGTAGGGATTACCAGCAGCAGGCATTTCCAGCAGAAACTAGATGCTCAGAGTCCAACTTTGCAGTCCTACAAGATGAATTCCCAACTTTTTTCCTATTGTCTGAGACAGTGGTCCAGAATCTGCAGTACTGCACAGAATCCTGGCTGTTGCTACACCCTATATACCCACTCATGTATTCCTGTATCATGAAATCCTTTCAAGTCTTCCTCTTGCTTACTTGTCCAGAGATTCCAGGCATTCCTGGGATACACATCTTCCCTAGTAATTATATCGAAGATTCCCCTAGGTGTCTACATGAGTCCCAACCAACTT... |
Task1_train_42122 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | GAAGATTCCCCTAGGTGTCTACATGAGTCCCAACCAACTTCTCTCCCACTTGTCATGTCTGGAGTCTGCTAGCAATACCTATTAGGAGGAATTACATGCCCTCCTTTCTGAATGACAGCATCCACAGTAACTGCAAAGTGGCTTATCTCTTAAAAAAAAAAAAAAAGCCTCCACACCAAAATAATTCCTCACCTCCTGTTTTTCTTCTAATTGAGGTAATGAGCAGGAGTGGGCTTCTACCAGTAATGATTTCAATGTGATTTTCTTACTAAAGGCACAAAGTAAGAATAACAACAGCAGCATTAGCAGAAACAACTTTG... | GAAGATTCCCCTAGGTGTCTACATGAGTCCCAACCAACTTCTCTCCCACTTGTCATGTCTGGAGTCTGCTAGCAATACCTATTAGGAGGAATTACATGCCCTCCTTTCTGAATGACAGCATCCACAGTAACTGCAAAGTGGCTTATCTCTTAAAAAAAAAAAAAAAGCCTCCACACCAAAATAATTCCTCACCTCCTGTTTTTCTTCTAATTGAGGTAATGAGCAGGAGTGGGCTTCTACCAGTAATGATTTCAATGTGATTTTCTTACTAAAGGCACAAAGTAAGAATAACAACAGCAGCATTAGCAGAAACAACTTTG... |
Task1_train_42123 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | GCACAATTTTTTAAAACAAAGCTAGATTAGTTTTGGCTTCTTAAACTTTGTATTCGGGTAGTTAAGCTGCCATACATGCTCAATAGGAATAGTATGTAATTTGAAAATACCGTAAAAAAATTTTTTTTCAAAGATACTTTAAAACATAATAGTAGACTTGAAAAAATGAAATTATTGGCCACCCTAGGGCCCTCTTGATGATGCAACCCACTGAAATGAGAATGATACAAGGGAGAAGTAGTTGGCCCTGGAGAACCCGTTCAGAATCAGAACAGGCCTCCTGCTTAAGGACCTCTCCAGGGACCTCCCTCACTCTCCAA... | GCACAATTTTTTAAAACAAAGCTAGATTAGTTTTGGCTTCTTAAACTTTGTATTCGGGTAGTTAAGCTGCCATACATGCTCAATAGGAATAGTATGTAATTTGAAAATACCGTAAAAAAATTTTTTTTCAAAGATACTTTAAAACATAATAGTAGACTTGAAAAAATGAAATTATTGGCCACCCTAGGGCCCTCTTGATGATGCAACCCACTGAAATGAGAATGATACAAGGGAGAAGTAGTTGGCCCTGGAGAACCCGTTCAGAATCAGAACAGGCCTCCTGCTTAAGGACCTCTCCAGGGACCTCCCTCACTCTCCAA... |
Task1_train_42124 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | GAGAACCCGTTCAGAATCAGAACAGGCCTCCTGCTTAAGGACCTCTCCAGGGACCTCCCTCACTCTCCAAGGCCTAGAGCTGAGATCAAGTCCCTCTGGCCATTATTATTTGGGAGGTAGATTCAAGGCTTCCCCTTGGACAGAAAGGCTATGGGGATATTTCCTCGCTCAGAAGTTTCACCCCTGCATTCTCTAAAGGAAGGACAAAGCCGATAGAAGCCCACAGAGCCCTCTCCTATCTGTGGCTTTTGCTCCACTCTTGGAAAGGATGCCATACAGGGATCCTCCATTCAGGGCATCTCGTTGGCCTAGGGAGCCCA... | GAGAACCCGTTCAGAATCAGAACAGGCCTCCTGCTTAAGGACCTCTCCAGGGACCTCCCTCACTCTCCAAGGCCTAGAGCTGAGATCAAGTCCCTCTGGCCATTATTATTTGGGAGGTAGATTCAAGGCTTCCCCTTGGACAGAAAGGCTATGGGGATATTTCCTCGCTCAGAAGTTTCACCCCTGCATTCTCTAAAGGAAGGACAAAGCCGATAGAAGCCCACAGAGCCCTCTCCTATCTGTGGCTTTTGCTCCACTCTTGGAAAGGATGCCATACAGGGATCCTCCATTCAGGGCATCTCGTTGGCCTAGGGAGCCCA... |
Task1_train_42125 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | TTTGGGAGGTAGATTCAAGGCTTCCCCTTGGACAGAAAGGCTATGGGGATATTTCCTCGCTCAGAAGTTTCACCCCTGCATTCTCTAAAGGAAGGACAAAGCCGATAGAAGCCCACAGAGCCCTCTCCTATCTGTGGCTTTTGCTCCACTCTTGGAAAGGATGCCATACAGGGATCCTCCATTCAGGGCATCTCGTTGGCCTAGGGAGCCCAAGTGAAGGCAAATTTCCTTCTCATTCAAATCAATCTTCTCCTAAAACTACCCACTCTGGGAACCCACGAGGGTACAAGTCATGAATCGAGATCAGATTCTCATTGATA... | TTTGGGAGGTAGATTCAAGGCTTCCCCTTGGACAGAAAGGCTATGGGGATATTTCCTCGCTCAGAAGTTTCACCCCTGCATTCTCTAAAGGAAGGACAAAGCCGATAGAAGCCCACAGAGCCCTCTCCTATCTGTGGCTTTTGCTCCACTCTTGGAAAGGATGCCATACAGGGATCCTCCATTCAGGGCATCTCGTTGGCCTAGGGAGCCCAAGTGAAGGCAAATTTCCTTCTCATTCAAATCAATCTTCTCCTAAAACTACCCACTCTGGGAACCCACGAGGGTACAAGTCATGAATCGAGATCAGATTCTCATTGATA... |
Task1_train_42126 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | GGCTTTTGCTCCACTCTTGGAAAGGATGCCATACAGGGATCCTCCATTCAGGGCATCTCGTTGGCCTAGGGAGCCCAAGTGAAGGCAAATTTCCTTCTCATTCAAATCAATCTTCTCCTAAAACTACCCACTCTGGGAACCCACGAGGGTACAAGTCATGAATCGAGATCAGATTCTCATTGATAACCTTCTTGAGTTAACCATCAAGGGGAGGGGGACTAGCCACTTTACCTTCCTCTGATCTAGACTAAATCCTCTAACTGTCCATTTTACCAGGTGTTCTTTTATTTCTCACCCCTATTTTTGGTCTTTAACTTCCT... | GGCTTTTGCTCCACTCTTGGAAAGGATGCCATACAGGGATCCTCCATTCAGGGCATCTCGTTGGCCTAGGGAGCCCAAGTGAAGGCAAATTTCCTTCTCATTCAAATCAATCTTCTCCTAAAACTACCCACTCTGGGAACCCACGAGGGTACAAGTCATGAATCGAGATCAGATTCTCATTGATAACCTTCTTGAGTTAACCATCAAGGGGAGGGGGACTAGCCACTTTACCTTCCTCTGATCTAGACTAAATCCTCTAACTGTCCATTTTACCAGGTGTTCTTTTATTTCTCACCCCTATTTTTGGTCTTTAACTTCCT... |
Task1_train_42127 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | GGGCATCTCGTTGGCCTAGGGAGCCCAAGTGAAGGCAAATTTCCTTCTCATTCAAATCAATCTTCTCCTAAAACTACCCACTCTGGGAACCCACGAGGGTACAAGTCATGAATCGAGATCAGATTCTCATTGATAACCTTCTTGAGTTAACCATCAAGGGGAGGGGGACTAGCCACTTTACCTTCCTCTGATCTAGACTAAATCCTCTAACTGTCCATTTTACCAGGTGTTCTTTTATTTCTCACCCCTATTTTTGGTCTTTAACTTCCTTCTGATGCATAAAAATATCCAAGTTTGATTTGGCTTTTTCCAAATCTTTT... | GGGCATCTCGTTGGCCTAGGGAGCCCAAGTGAAGGCAAATTTCCTTCTCATTCAAATCAATCTTCTCCTAAAACTACCCACTCTGGGAACCCACGAGGGTACAAGTCATGAATCGAGATCAGATTCTCATTGATAACCTTCTTGAGTTAACCATCAAGGGGAGGGGGACTAGCCACTTTACCTTCCTCTGATCTAGACTAAATCCTCTAACTGTCCATTTTACCAGGTGTTCTTTTATTTCTCACCCCTATTTTTGGTCTTTAACTTCCTTCTGATGCATAAAAATATCCAAGTTTGATTTGGCTTTTTCCAAATCTTTT... |
Task1_train_42128 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | AAAAAAAATTCATGTGCACTTGGCTTCTCACAGCATGACTGTTAGGCTCCTGGAGGGACCATCCTAAGAACAAGCATTCTAAGGGGCGGGAAGCAGAAACTGCCAGGCTAGCCAAGGGTTATGCCTGGGACTGGCATAGTGTCACTTCCACCATATTCTGTTGACCCATGTAGTCATAGGGTCTGCCCAAATTCAAGGAGCTGGAAGAAGAGACACCACCTTTTGATGGGGAGTGGCAAGGTCACATAGCAGAGAATTGTAGGATGGGAGATATTGCTGTGATTTTCTTTGGAAAATCTGCCTCAGTGAGGCACTTCATG... | AAAAAAAATTCATGTGCACTTGGCTTCTCACAGCATGACTGTTAGGCTCCTGGAGGGACCATCCTAAGAACAAGCATTCTAAGGGGCGGGAAGCAGAAACTGCCAGGCTAGCCAAGGGTTATGCCTGGGACTGGCATAGTGTCACTTCCACCATATTCTGTTGACCCATGTAGTCATAGGGTCTGCCCAAATTCAAGGAGCTGGAAGAAGAGACACCACCTTTTGATGGGGAGTGGCAAGGTCACATAGCAGAGAATTGTAGGATGGGAGATATTGCTGTGATTTTCTTTGGAAAATCTGCCTCAGTGAGGCACTTCATG... |
Task1_train_42129 | Here is a mutation located on Chromosome 12. Determine whether it’s benign or pathogenic. If the latter, what disease does it cause? | Benign | TTGGCCTCCCAAAGTGCTGGGATTAGAGGCGTGAGCCACCCTGGTGAGCCCCTTCCTACTTTTTTTTTTTTTTCTTTTTGGTGAGACAGGGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGCACCATCTTGGCTCACTGCAACCTCTGCCTCCTGGGCTCAAGCATTCCTCCCGCCACAGCCTCCCCAATGCACAGCTAACTTTTGTATTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGGTCAAACTCCTGGCCTCAGACGATCTTCCCACCCTGGCTTTCTAAAATGCTGGGATTACAGGCATGAG... | TTGGCCTCCCAAAGTGCTGGGATTAGAGGCGTGAGCCACCCTGGTGAGCCCCTTCCTACTTTTTTTTTTTTTTCTTTTTGGTGAGACAGGGTCTCACTCTGTCTCCCAGGCTGGAGTGCAGTGGCACCATCTTGGCTCACTGCAACCTCTGCCTCCTGGGCTCAAGCATTCCTCCCGCCACAGCCTCCCCAATGCACAGCTAACTTTTGTATTTTTTGTAGAGATGGGGTTTCGCCATGTTGCCCAGGCTGGGTCAAACTCCTGGCCTCAGACGATCTTCCCACCCTGGCTTTCTAAAATGCTGGGATTACAGGCATGAG... |
Task1_train_42130 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | ACTGAGTCTGGGAGAAGCCCCCGCGCCCGCGGAGCCGGCAGCTAAATTTACCCCGGCTGACTCAGCCCTTGCCCGGAATGGGGGGTGGGGGGAGGGCGCCAGGGCAGTGGGAAGAGCCGACAGGGGTGGGCTGGGGGCAAGGAAGGGAGAGTCCCGGCTGGGGGAGAAAAGAGGTGGGCCAGGAGCTCCCAACGAAGAAAGCAGCCCCCTCCCCTCACACAGAGCGGGAAGTAGCAGAGGAGTCCCGGGGGAGGGCCACTGTGGGGAAAGGGTCAGTGAAAGGAAGACGATGCCAAGGCTGGATAAAGGGAAGCTTAGAT... | ACTGAGTCTGGGAGAAGCCCCCGCGCCCGCGGAGCCGGCAGCTAAATTTACCCCGGCTGACTCAGCCCTTGCCCGGAATGGGGGGTGGGGGGAGGGCGCCAGGGCAGTGGGAAGAGCCGACAGGGGTGGGCTGGGGGCAAGGAAGGGAGAGTCCCGGCTGGGGGAGAAAAGAGGTGGGCCAGGAGCTCCCAACGAAGAAAGCAGCCCCCTCCCCTCACACAGAGCGGGAAGTAGCAGAGGAGTCCCGGGGGAGGGCCACTGTGGGGAAAGGGTCAGTGAAAGGAAGACGATGCCAAGGCTGGATAAAGGGAAGCTTAGAT... |
Task1_train_42131 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TGCACTATTAGGGCTTTATTATTTGAAGTTATTGGCCCACATTAACTTGGAGAATTAACTTTCAGATATCTAATTAACACATTAGAGTGAATAAATGTATCAGGCTTTTCCAACATGACATTCAGCTTAAAATAGGTTTGGAAAGAAGGTAAAGAACTAAGTCTAGCATAGGGCTGCTTGCTTTGAGAGGAGATTTGTTTTGGGAACCCTGGGCAGAAGAGGCATAATGGCACTAGACACATACCAAGGAGCGGAGGGCACATGAAAAACTGATGCATTTGGAATATTCACCATTTTATGTTAGTTACATAAGATTCAGC... | TGCACTATTAGGGCTTTATTATTTGAAGTTATTGGCCCACATTAACTTGGAGAATTAACTTTCAGATATCTAATTAACACATTAGAGTGAATAAATGTATCAGGCTTTTCCAACATGACATTCAGCTTAAAATAGGTTTGGAAAGAAGGTAAAGAACTAAGTCTAGCATAGGGCTGCTTGCTTTGAGAGGAGATTTGTTTTGGGAACCCTGGGCAGAAGAGGCATAATGGCACTAGACACATACCAAGGAGCGGAGGGCACATGAAAAACTGATGCATTTGGAATATTCACCATTTTATGTTAGTTACATAAGATTCAGC... |
Task1_train_42132 | This genomic variant is located on Chromosome 12. Can you determine its pathogenicity and name any linked disease? | Benign | CACTGGAGGTCAGGAGTCTGAGACCAGCCTGACCATCATGGTGAAACCCAGTCTCCACTAAAAATACAAAAATTAGTCAGGTGTGGTGGTGGATGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAAGCTCTTGAACCCAGGAGGTTGAGGTTGCAGTGAGCCCAGATCGTACCACTGCACTCCAGCCTGGGCAACAGAACAAGACTCCATCTCACAAAAAAAAAAAAAAAAAAAAAAAGTACATGATGCTCTGTAATGGTAATCTTTAGATATACATTTTGTGTTTCATAAATAAAAGTTTTAAATTACTAA... | CACTGGAGGTCAGGAGTCTGAGACCAGCCTGACCATCATGGTGAAACCCAGTCTCCACTAAAAATACAAAAATTAGTCAGGTGTGGTGGTGGATGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAAGCTCTTGAACCCAGGAGGTTGAGGTTGCAGTGAGCCCAGATCGTACCACTGCACTCCAGCCTGGGCAACAGAACAAGACTCCATCTCACAAAAAAAAAAAAAAAAAAAAAAAGTACATGATGCTCTGTAATGGTAATCTTTAGATATACATTTTGTGTTTCATAAATAAAAGTTTTAAATTACTAA... |
Task1_train_42133 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | GACATTTTTAGAAGGCCTTAAGGTGGGATAATTAACAACGATATCAAGGATTACAGGACAGTCTAATATGGTTGATGTATTTAGTGTTTACCTCAAGCTGTGACAGTTTTTATTAAAATTAAATTTCTGTATTATAAGTTTAATTCAAAAGGCAGTTATATGTTATCTATGTAACAGAATTTGCCAAATAGCAACTAAGTTGCTGTTAATTGTTTTATGGGACGAAAGCAGCCAGTCTTGGCCCTTCTGTCTTAGGGATGGATTATATTTGGATCATGTTGAATATATTTTTCCCTTATTCTTTCAGATTCATCAGGATT... | GACATTTTTAGAAGGCCTTAAGGTGGGATAATTAACAACGATATCAAGGATTACAGGACAGTCTAATATGGTTGATGTATTTAGTGTTTACCTCAAGCTGTGACAGTTTTTATTAAAATTAAATTTCTGTATTATAAGTTTAATTCAAAAGGCAGTTATATGTTATCTATGTAACAGAATTTGCCAAATAGCAACTAAGTTGCTGTTAATTGTTTTATGGGACGAAAGCAGCCAGTCTTGGCCCTTCTGTCTTAGGGATGGATTATATTTGGATCATGTTGAATATATTTTTCCCTTATTCTTTCAGATTCATCAGGATT... |
Task1_train_42134 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGCGTCCTGCAGTGTCTGCAGCTGGCTGGCCTGCACGACAGCCTTGCGCTGTACCCCGAGTTTGCCCCGCGCTTCAGTCGTGGCCTCCGAGGGGAGCTCAGCTACAACCTGGGTGCTGGGGGAGGCTCTGCAGAGGTGAGTGTGCTGAGTATGTGCTTGGAGGGGATGGGGGTGCCAGGGAGCCTGGTGAAGTGGGCAGAGGCTGGGGATGGTGGAGAGCTGTGTGTGAAGTGTGGCCTGGTATGAAAGCTCCCACCTTGGGCAGGGGTCTACACCCTCTCTGCCCTTCCACACTCATGTGCCCAGCCCAGCATGTGCAG... | TGCGTCCTGCAGTGTCTGCAGCTGGCTGGCCTGCACGACAGCCTTGCGCTGTACCCCGAGTTTGCCCCGCGCTTCAGTCGTGGCCTCCGAGGGGAGCTCAGCTACAACCTGGGTGCTGGGGGAGGCTCTGCAGAGGTGAGTGTGCTGAGTATGTGCTTGGAGGGGATGGGGGTGCCAGGGAGCCTGGTGAAGTGGGCAGAGGCTGGGGATGGTGGAGAGCTGTGTGTGAAGTGTGGCCTGGTATGAAAGCTCCCACCTTGGGCAGGGGTCTACACCCTCTCTGCCCTTCCACACTCATGTGCCCAGCCCAGCATGTGCAG... |
Task1_train_42135 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | AGCCTTGGTAGGGGAGGTGAGTGGGACACAATAGTGACCATCCATGCCGATTCCCTGTCCCTCACTATCCCTAGGTGGACACCAGCTCCCTGAGCGGCGACAATACCCTTATGTCCACGCTGGAGGAGAAGGAGACAGATGGGGAGCAGGGCCCCACGGTCTCCCCAGCCCCAGCTGATGAGCCCTCCAGCCCCCTGCTGTCCCCTGGCTGCACCTCCTCATCCTCAGCTGCCAAGCTGCTATCCCCACGTCGAACAGCACCCCGGCCTCGTCTAGGTGGCAGAGGGAGGCCAGGCAGGGCAGGGGCTTTGAAGGCTGAG... | AGCCTTGGTAGGGGAGGTGAGTGGGACACAATAGTGACCATCCATGCCGATTCCCTGTCCCTCACTATCCCTAGGTGGACACCAGCTCCCTGAGCGGCGACAATACCCTTATGTCCACGCTGGAGGAGAAGGAGACAGATGGGGAGCAGGGCCCCACGGTCTCCCCAGCCCCAGCTGATGAGCCCTCCAGCCCCCTGCTGTCCCCTGGCTGCACCTCCTCATCCTCAGCTGCCAAGCTGCTATCCCCACGTCGAACAGCACCCCGGCCTCGTCTAGGTGGCAGAGGGAGGCCAGGCAGGGCAGGGGCTTTGAAGGCTGAG... |
Task1_train_42136 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | GTCAGGTGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTATCCAGGTGTGGTGGTGGGTACCTATAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATAGCTTGAACCTGGGAGGTGGAGGTTGTAGTGAGCCAAGATTGTGCCACCGCACTCCAGCCTGGGCAAAAGAGCGAGACTCTGTCTCAAAGCAAACACATTTTGAGGGATTATGAGGGAAAATGGATTCTAAGCTAGACTTCCACATCCAAGCAAACAGTCAATTAAGAGTGAGGATAGATATTAAGTAAAGAC... | GTCAGGTGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATGCAAAAATTATCCAGGTGTGGTGGTGGGTACCTATAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATAGCTTGAACCTGGGAGGTGGAGGTTGTAGTGAGCCAAGATTGTGCCACCGCACTCCAGCCTGGGCAAAAGAGCGAGACTCTGTCTCAAAGCAAACACATTTTGAGGGATTATGAGGGAAAATGGATTCTAAGCTAGACTTCCACATCCAAGCAAACAGTCAATTAAGAGTGAGGATAGATATTAAGTAAAGAC... |
Task1_train_42137 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | CTATAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATAGCTTGAACCTGGGAGGTGGAGGTTGTAGTGAGCCAAGATTGTGCCACCGCACTCCAGCCTGGGCAAAAGAGCGAGACTCTGTCTCAAAGCAAACACATTTTGAGGGATTATGAGGGAAAATGGATTCTAAGCTAGACTTCCACATCCAAGCAAACAGTCAATTAAGAGTGAGGATAGATATTAAGTAAAGACATTTTCAGACAACCAGGGTCTCAGTGACTTAACCTCCCATGCAATCGTTGTCAGAAAGTGAGTGGAGGAGGGACTCTACTAAAACAAG... | CTATAATCCCAGCTACTCGGGAGACTGAGGCAGGAGAATAGCTTGAACCTGGGAGGTGGAGGTTGTAGTGAGCCAAGATTGTGCCACCGCACTCCAGCCTGGGCAAAAGAGCGAGACTCTGTCTCAAAGCAAACACATTTTGAGGGATTATGAGGGAAAATGGATTCTAAGCTAGACTTCCACATCCAAGCAAACAGTCAATTAAGAGTGAGGATAGATATTAAGTAAAGACATTTTCAGACAACCAGGGTCTCAGTGACTTAACCTCCCATGCAATCGTTGTCAGAAAGTGAGTGGAGGAGGGACTCTACTAAAACAAG... |
Task1_train_42138 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACCAGGCCATTCCGGGGCCCACAGGCTGGCCAGGGGCTCTTGGGGTCAGAAGACACCGGCTGGAAATCCCCGTACTCAGGCTTGGGCTCCCGCCAGCTCTTGGATGGCAGCTCCTTGCCATCCACCCTATGGGCAACAGTGCAGATATAGGTGAGGGTGGTCTTGCCTGCCCAGACATTCCAGCCTTGCACCCGCCAATGGTGCTGGGCTTAGGGAGGCACTTCCTGCCATCCACCCCCGGGGAAGGGGACATGTCGCTAGTGATTGCTCCCAACACCCTTCTTGACACTGGCAACAGGCAAGGACCTTAGGGAACCCCA... | ACCAGGCCATTCCGGGGCCCACAGGCTGGCCAGGGGCTCTTGGGGTCAGAAGACACCGGCTGGAAATCCCCGTACTCAGGCTTGGGCTCCCGCCAGCTCTTGGATGGCAGCTCCTTGCCATCCACCCTATGGGCAACAGTGCAGATATAGGTGAGGGTGGTCTTGCCTGCCCAGACATTCCAGCCTTGCACCCGCCAATGGTGCTGGGCTTAGGGAGGCACTTCCTGCCATCCACCCCCGGGGAAGGGGACATGTCGCTAGTGATTGCTCCCAACACCCTTCTTGACACTGGCAACAGGCAAGGACCTTAGGGAACCCCA... |
Task1_train_42139 | This mutation on Chromosome 12 may be significant. Is it associated with any clinical condition, or is it benign? | Benign | CAGCCCCGTGTTGGGCCCTGGGGCTGGGCCACCAGGCCGTGGCCGGGCCCGGCTGCTTAGGTAGGCCTTCTCCTCTTCCAGTGCCCGACGCAGGTCTTCCGCCTTGGCCATCAGCTTGGAGATGTTGAGGCTCTCGGCCTCCAGCTTCCGGGCTTCCATCTTGACTTCCCTCCGGAGCGGGGAGCCCCCGCCAGCCCCCTCCTTGTTCTTGGTGGCCTCTGTGCGGCGGTTCAGCGCTGGCAGCTTGCTCTTCTTAAGGCCGAACCAGCTGGCGATGCTGCTGGTGTTGCGGTGCTTGACCTCGGCGCCAGGGGCTCGCT... | CAGCCCCGTGTTGGGCCCTGGGGCTGGGCCACCAGGCCGTGGCCGGGCCCGGCTGCTTAGGTAGGCCTTCTCCTCTTCCAGTGCCCGACGCAGGTCTTCCGCCTTGGCCATCAGCTTGGAGATGTTGAGGCTCTCGGCCTCCAGCTTCCGGGCTTCCATCTTGACTTCCCTCCGGAGCGGGGAGCCCCCGCCAGCCCCCTCCTTGTTCTTGGTGGCCTCTGTGCGGCGGTTCAGCGCTGGCAGCTTGCTCTTCTTAAGGCCGAACCAGCTGGCGATGCTGCTGGTGTTGCGGTGCTTGACCTCGGCGCCAGGGGCTCGCT... |
Task1_train_42140 | Consider this mutation on Chromosome 12. Is this a benign change or a disease-causing variant? | Benign | TGAAGATCCTCAATCTCATTTGCAAAGCCCCTTTTGCTAAAGGAGGTGGACATCTTGGGGGACCATTATTCATCCTACCACAGCCCCATGTATGTTTCTGTGCGCTGCCTTGGTGGAGTGAGAGGAGAGAGCACCCAGCAGGGTTACAGGGTTTCAAAGTGTTCCTAAATTAAGATCTTGTGGGTAAACTCAGCTCTGTATCTACTGTGATAACTGAGACCATCATAAACTAGCCTCATTTCCATTAGTTCCATATCCCTCCCTCCCAACACTGCTTCCTTTAAAATGCTCTGTAGCACTGAAGCTGGACTCCTTATTAC... | TGAAGATCCTCAATCTCATTTGCAAAGCCCCTTTTGCTAAAGGAGGTGGACATCTTGGGGGACCATTATTCATCCTACCACAGCCCCATGTATGTTTCTGTGCGCTGCCTTGGTGGAGTGAGAGGAGAGAGCACCCAGCAGGGTTACAGGGTTTCAAAGTGTTCCTAAATTAAGATCTTGTGGGTAAACTCAGCTCTGTATCTACTGTGATAACTGAGACCATCATAAACTAGCCTCATTTCCATTAGTTCCATATCCCTCCCTCCCAACACTGCTTCCTTTAAAATGCTCTGTAGCACTGAAGCTGGACTCCTTATTAC... |
Task1_train_42141 | Given this context: Chromosome 12 — does this variant present pathogenic behavior, and if so, what disease does it relate to? | Benign | AGAAGGTCTTTAAGCAGAAGAATGGTCAGAGTCACACAACTCGAACTAAAGGTGGGGAGAAACTGCAGGGAGGCAGGGAGACCAGTTGAGAGGCTGTTGTTTAGGCAAAAGAGGAGGGCAGTGGCAGAAAGAGGAGGACAGTGGCTGTTGTTTAGGCCAGTCTGAGGGCAGTGGCAGAAGGATGGAGAGGGGCTAGAGCTCAAGACTCTGCTTCTGAGGCCTCTTTGTCCCTGGCAGCAAAGCTGAGGCCAAAGGTTCCACATCACTCAGTTCTGCTAGAACCTGACACCCTGCCTCACATCCCCAACACACTCTAGGGT... | AGAAGGTCTTTAAGCAGAAGAATGGTCAGAGTCACACAACTCGAACTAAAGGTGGGGAGAAACTGCAGGGAGGCAGGGAGACCAGTTGAGAGGCTGTTGTTTAGGCAAAAGAGGAGGGCAGTGGCAGAAAGAGGAGGACAGTGGCTGTTGTTTAGGCCAGTCTGAGGGCAGTGGCAGAAGGATGGAGAGGGGCTAGAGCTCAAGACTCTGCTTCTGAGGCCTCTTTGTCCCTGGCAGCAAAGCTGAGGCCAAAGGTTCCACATCACTCAGTTCTGCTAGAACCTGACACCCTGCCTCACATCCCCAACACACTCTAGGGT... |
Task1_train_42142 | This sequence change occurs on Chromosome 12. What is the medical significance of this variant — is it benign or linked to a disease? | Benign | GAATATCACAGCATGGTCACCTTGTGGTGGCTTGTGAACTACCACACACCACTTCTAGGCAACTTAACAATCTGCTTTTATACAGTTTATATGGTTCTGCATATGATTTCCTTTGAAAAGGGCCCCATGTCAAAAAGAAAAATATGAAATCCACTGAAGCAGGTAGGTAAGGGGTAGGAAATGGTTGAGGCCATCTCTTAAAAAACTCTTAACCCTATCATCCTTTAACAAAAGCCATTCCTAAGGGACAGGAAGAAGGTAGAACTTTCCTCTTGCGTCTAAGTCACATCTTAAAAGGTAAAACAGGCAGGCCAGGTGCG... | GAATATCACAGCATGGTCACCTTGTGGTGGCTTGTGAACTACCACACACCACTTCTAGGCAACTTAACAATCTGCTTTTATACAGTTTATATGGTTCTGCATATGATTTCCTTTGAAAAGGGCCCCATGTCAAAAAGAAAAATATGAAATCCACTGAAGCAGGTAGGTAAGGGGTAGGAAATGGTTGAGGCCATCTCTTAAAAAACTCTTAACCCTATCATCCTTTAACAAAAGCCATTCCTAAGGGACAGGAAGAAGGTAGAACTTTCCTCTTGCGTCTAAGTCACATCTTAAAAGGTAAAACAGGCAGGCCAGGTGCG... |
Task1_train_42143 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | TAACTCTTACTTCTAGAGATCTAGGCATGATTAGAACCCAACAGAGGACTAGAGAAAGTTAAGACTCACCGACCAGAGAAATCTAATTCCATAGCAGAATATACATAAATAAAATGTGAATCTCCACCTGGGTGGGCAAAGAGTAAAGGTTAGACAAATGTCCACTCAAACCAAAGCCTCTGAGGCTACGGAAGTCAAGATAGCAAATTTGGGGATAAGAGTTACTGGTGAGAAAGAGGATCAATTCCTAGAATAGGCAACTACTGTCATTTAAAAAGCCAAAGACAGGGGCCAGGAGTGGTGGCTCACACCTGTAATCC... | TAACTCTTACTTCTAGAGATCTAGGCATGATTAGAACCCAACAGAGGACTAGAGAAAGTTAAGACTCACCGACCAGAGAAATCTAATTCCATAGCAGAATATACATAAATAAAATGTGAATCTCCACCTGGGTGGGCAAAGAGTAAAGGTTAGACAAATGTCCACTCAAACCAAAGCCTCTGAGGCTACGGAAGTCAAGATAGCAAATTTGGGGATAAGAGTTACTGGTGAGAAAGAGGATCAATTCCTAGAATAGGCAACTACTGTCATTTAAAAAGCCAAAGACAGGGGCCAGGAGTGGTGGCTCACACCTGTAATCC... |
Task1_train_42144 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | AGAGGTGGCAGCTCTGCTACATAAAAACCTTTGTCCTACTTAAGCTTAAGTCCTGGTCCTCTTATTTTCTTGCTGTGAGACTTTGGGATAGTTGCTTAATTTATCTGCACTTCTTTCTCCTCATTTCTAAAACAGGGATAATAACACAGGGTTGTGAGAATTGTAAAACACAGTATATATGGAAGCACTTTATAAATTGTGATGCAGTATGCAACTGTAATGATAGCCAGCATTTACTAAATACTTAGTGAATGTCAGACACTGAACTAAGCATTTTCCATATATTAGCTGATTTGGTATTTATAACAACCTTATGCGGT... | AGAGGTGGCAGCTCTGCTACATAAAAACCTTTGTCCTACTTAAGCTTAAGTCCTGGTCCTCTTATTTTCTTGCTGTGAGACTTTGGGATAGTTGCTTAATTTATCTGCACTTCTTTCTCCTCATTTCTAAAACAGGGATAATAACACAGGGTTGTGAGAATTGTAAAACACAGTATATATGGAAGCACTTTATAAATTGTGATGCAGTATGCAACTGTAATGATAGCCAGCATTTACTAAATACTTAGTGAATGTCAGACACTGAACTAAGCATTTTCCATATATTAGCTGATTTGGTATTTATAACAACCTTATGCGGT... |
Task1_train_42145 | A mutation found on Chromosome 12 may be clinically relevant. Is it pathogenic or benign, and if the former, which disease is implicated? | Benign | CTCAGCCTCCCAAAGTGATGGGATTACAGTTGCCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGAAGGGGTTTCACCATGTTGGCCAGCTGATTTTTTGTATTTTTTTTAATAGAGATGAGGTTTCACCATGTTGGCCAGGGTGGTCTCGAACTCCTGACCTCAAGTAACCCACCTGCCTTGGCATCCCAAAGTGCTGGGGTTACAGGCATGAGCCACTGCACCCTGCCTATATTTACTTGTATTTTTTTATTTGTCTTTTCTGTTTATTTTTTATTTTTTCCTGAGATGGAGTCTTGCTCTGCCCCGCTGGCT... | CTCAGCCTCCCAAAGTGATGGGATTACAGTTGCCCACCACACCCAGCTAATTTTTGTATTTTTAGTAGAGAAGGGGTTTCACCATGTTGGCCAGCTGATTTTTTGTATTTTTTTTAATAGAGATGAGGTTTCACCATGTTGGCCAGGGTGGTCTCGAACTCCTGACCTCAAGTAACCCACCTGCCTTGGCATCCCAAAGTGCTGGGGTTACAGGCATGAGCCACTGCACCCTGCCTATATTTACTTGTATTTTTTTATTTGTCTTTTCTGTTTATTTTTTATTTTTTCCTGAGATGGAGTCTTGCTCTGCCCCGCTGGCT... |
Task1_train_42146 | The following genetic variant occurs on Chromosome 12. Classify its clinical effect — pathogenic or benign — and list any associated condition. | Benign | CTAATGTCTTCAGATTCCTCTGAAACTCTTTTCCTTCATATGACCGCTGTACATCTTTCAATACACTCTTCCACCTGGGAGATAATGTCATTGGAGTTTGGATGACCATTTTTTCTAGCTCTTTAGGTTGTGTTTCCTTCATCTGCATCTGATCCTTTGTTTTGATCTGCCTTTCGAGGTCCTCTAGCCCTCTCTCTGGCTTCTGCTTTTCCTTCCCTTTCTCCCTTCTCCTGTGTGGCCCCAAATGTTTCGCTTCCTTCTGAATCTGCCTCATCTGTCCATTCTCCTTTTCCAAGAGCAACCCTTGTGTTTTCATTTTT... | CTAATGTCTTCAGATTCCTCTGAAACTCTTTTCCTTCATATGACCGCTGTACATCTTTCAATACACTCTTCCACCTGGGAGATAATGTCATTGGAGTTTGGATGACCATTTTTTCTAGCTCTTTAGGTTGTGTTTCCTTCATCTGCATCTGATCCTTTGTTTTGATCTGCCTTTCGAGGTCCTCTAGCCCTCTCTCTGGCTTCTGCTTTTCCTTCCCTTTCTCCCTTCTCCTGTGTGGCCCCAAATGTTTCGCTTCCTTCTGAATCTGCCTCATCTGTCCATTCTCCTTTTCCAAGAGCAACCCTTGTGTTTTCATTTTT... |
Task1_train_42147 | This is a variant located on Chromosome 12. Is this mutation a likely cause of disease or not? | Benign | GGCCAAGATGGTGAAATTCCATCTCTACTAAAAATACAAAAATTAACCATGCGTGGTGGCATGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGTAGTGAGCTGAGATCACACCACTGCACTCCAACCTGGGCGACAGAGTAAGACTCTGTCTCAAAAAAAAAAAAAAAGTTAAAACTCAATTTCAAAAATGGGCAAGTACTTGAATAGATATTTCACCAAAAAATGTATGGAAATAGCTTAATAAGCACATGAAACATGCTCAGCATCATTTGCCATTAGGA... | GGCCAAGATGGTGAAATTCCATCTCTACTAAAAATACAAAAATTAACCATGCGTGGTGGCATGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATCGCTTGAACCCAGGAGGTGGAGGTTGTAGTGAGCTGAGATCACACCACTGCACTCCAACCTGGGCGACAGAGTAAGACTCTGTCTCAAAAAAAAAAAAAAAGTTAAAACTCAATTTCAAAAATGGGCAAGTACTTGAATAGATATTTCACCAAAAAATGTATGGAAATAGCTTAATAAGCACATGAAACATGCTCAGCATCATTTGCCATTAGGA... |
Task1_train_42148 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | TGTGGTCTCATCTGAAGGTGTGATCGGGGAAGATCTGCCTCTAAGCAGATCATGCGGTGTTGCATGATTCAGCTTTTCGTGGCTGTTCAACTGAGGACTTCAGTTCCTCAATGGCTCTTGCTGGCAGCCTCTCTACAGGGCCACAGGGCAGCTTACAACATGGCAGCAGCTTTACCTTAGAGCAACAGGACTGCAGAGAGTGCTCAGGACAGAAGTCACAATCTTTTTATAACCTAATCTTGAAAGTGGTAGCCCATCACCTCTACTTTCTATTTACTAGAAGTGAGTCACGAAATCCAGCCAACACTAAAGGAGAGGGA... | TGTGGTCTCATCTGAAGGTGTGATCGGGGAAGATCTGCCTCTAAGCAGATCATGCGGTGTTGCATGATTCAGCTTTTCGTGGCTGTTCAACTGAGGACTTCAGTTCCTCAATGGCTCTTGCTGGCAGCCTCTCTACAGGGCCACAGGGCAGCTTACAACATGGCAGCAGCTTTACCTTAGAGCAACAGGACTGCAGAGAGTGCTCAGGACAGAAGTCACAATCTTTTTATAACCTAATCTTGAAAGTGGTAGCCCATCACCTCTACTTTCTATTTACTAGAAGTGAGTCACGAAATCCAGCCAACACTAAAGGAGAGGGA... |
Task1_train_42149 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | ACAAAGGCATACACAATCTGACCACATCTCACACACACAGAAATACACACACCCCAACTGTGTTTTTCTCCTCCTAATATCACCTTCCACTAAAATATCTGGGGAATAAGGACTTTGTTTCTTGTCAGCCCTCAGAGATCAGCTCATGCTGCAATTTGTTTCTCCAATATCACCTCCTCCACCCCAATTTCGGCACAGCTCTGAGACTCTGCTCCCTTCCCCACATGTTACCATGTGTAAGCCCCAAACTCATATACTCCTTTTATCTAATGCTGCCAACTGCACCAGCCTCGGAAGGATGGTATGAGCAAGGCAACTGT... | ACAAAGGCATACACAATCTGACCACATCTCACACACACAGAAATACACACACCCCAACTGTGTTTTTCTCCTCCTAATATCACCTTCCACTAAAATATCTGGGGAATAAGGACTTTGTTTCTTGTCAGCCCTCAGAGATCAGCTCATGCTGCAATTTGTTTCTCCAATATCACCTCCTCCACCCCAATTTCGGCACAGCTCTGAGACTCTGCTCCCTTCCCCACATGTTACCATGTGTAAGCCCCAAACTCATATACTCCTTTTATCTAATGCTGCCAACTGCACCAGCCTCGGAAGGATGGTATGAGCAAGGCAACTGT... |
Task1_train_42150 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | CTTCTTTTTCTAGGTGTTCTCTATTCTATGTATAAGGATTACATTAGACCACGATTCTTCAGTGAGTCCAAAAAATGAAGCTTACATGCTGGAAGCAAGAAAGACAAGAAGCTTCTGAAAACTATTTATTATGAAGAATAAATTTTCAATATGTAGCAAATTTTACTACACAAGTGTCACAGAATGCTCATAGCCTTTGTATTTCAAGTCTCAGTGTTTTAAGAAGTTGATTTCCAGATCAACAATCATAAACAGTCAACTCAGAAATATCCCGTGTTAATGTCTTTCAGAACCTAGGGCATGATTTTCTGACTTAATTT... | CTTCTTTTTCTAGGTGTTCTCTATTCTATGTATAAGGATTACATTAGACCACGATTCTTCAGTGAGTCCAAAAAATGAAGCTTACATGCTGGAAGCAAGAAAGACAAGAAGCTTCTGAAAACTATTTATTATGAAGAATAAATTTTCAATATGTAGCAAATTTTACTACACAAGTGTCACAGAATGCTCATAGCCTTTGTATTTCAAGTCTCAGTGTTTTAAGAAGTTGATTTCCAGATCAACAATCATAAACAGTCAACTCAGAAATATCCCGTGTTAATGTCTTTCAGAACCTAGGGCATGATTTTCTGACTTAATTT... |
Task1_train_42151 | A change on Chromosome 12 is being evaluated. Identify whether the variant is neutral or disease-linked. Mention the disease if applicable. | Benign | TTCTTAGTTTCAAGTATGAATCTATTCAAACATGTTTACTGAACACCTACTATGTGCTAAGTAAGGCACCTAGTGTTGGAGGTGCAGCAATGAACAAGGCAGAGAAGATGCTTACCCTCATTCTAGTTCAGGGAGCTGTCAAACAAGGACACAAATACATAAACACTGTAAGTGACAGATGCTACAAAGAAAATACAAGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGCGGATCACTTGAGGCCAGGAGTTGAAGACCAGCCTGACCAACATAGTGAGATCCCGTCTCTACTAA... | TTCTTAGTTTCAAGTATGAATCTATTCAAACATGTTTACTGAACACCTACTATGTGCTAAGTAAGGCACCTAGTGTTGGAGGTGCAGCAATGAACAAGGCAGAGAAGATGCTTACCCTCATTCTAGTTCAGGGAGCTGTCAAACAAGGACACAAATACATAAACACTGTAAGTGACAGATGCTACAAAGAAAATACAAGGCCGGGTGCAGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGCTGGCGGATCACTTGAGGCCAGGAGTTGAAGACCAGCCTGACCAACATAGTGAGATCCCGTCTCTACTAA... |
Task1_train_42152 | A variant affecting Chromosome 12 has been observed. Determine if it's benign or associated with disease. | Benign | TGCGAAGCCTGCAGGCTGGACGGTGATCTGTGGGGGGGTGTCCACTGGCTTGGGGGTAGGGGCAGCAGCGGTGGCAGCAGTGGGCTGCGGGAGGATGGCAGGTGTGGTCTGCAGCAGCGGCTGGGTCTGGAACAGCGTCTGGGGCTGGGCTGGTGGCCGGGGTTGGGCCGTCGAGGAGGCCTGTACTGGTGCGGCAGCTTGTACCGGTGCCGGAAGAGCGGTGTTCAGCACAGCAGCTGCTATGGAGCAAGGCAGAGACAGAGGTGCTCAAATGCCTAGCCACTGCTCACAGCGGCTCCAATCCCAAGGGATCTGGCACA... | TGCGAAGCCTGCAGGCTGGACGGTGATCTGTGGGGGGGTGTCCACTGGCTTGGGGGTAGGGGCAGCAGCGGTGGCAGCAGTGGGCTGCGGGAGGATGGCAGGTGTGGTCTGCAGCAGCGGCTGGGTCTGGAACAGCGTCTGGGGCTGGGCTGGTGGCCGGGGTTGGGCCGTCGAGGAGGCCTGTACTGGTGCGGCAGCTTGTACCGGTGCCGGAAGAGCGGTGTTCAGCACAGCAGCTGCTATGGAGCAAGGCAGAGACAGAGGTGCTCAAATGCCTAGCCACTGCTCACAGCGGCTCCAATCCCAAGGGATCTGGCACA... |
Task1_train_42153 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | TTCAAGCGATTCCCATGCCTCAGCCTCCTGAGTAGTTGGGATTACAGGCGTGCACCACCACGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGATGATCCGCCCACCTCGACCTCCCAAACTGCTGGCATTACAAGCATGAGCCACCACGCCCGGCCTCTTTCTTTCTTTTGAATTAGCAATGGGGTCTCACTATGTTCCCCAGGCAGGTCTCAAACACCTAGCCTCAAGAGATCCTCCTGTCTCAGTCTCCCAAAGTCCTGGGATTACCG... | TTCAAGCGATTCCCATGCCTCAGCCTCCTGAGTAGTTGGGATTACAGGCGTGCACCACCACGCCTGGCTAATTTTTTTGTATTTTTAGTAGAGATGGAGTTTCACCATGTTGGCCAGGCTGGTCTCAAACTCCTGACCTCAGATGATCCGCCCACCTCGACCTCCCAAACTGCTGGCATTACAAGCATGAGCCACCACGCCCGGCCTCTTTCTTTCTTTTGAATTAGCAATGGGGTCTCACTATGTTCCCCAGGCAGGTCTCAAACACCTAGCCTCAAGAGATCCTCCTGTCTCAGTCTCCCAAAGTCCTGGGATTACCG... |
Task1_train_42154 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | CAGAGTATCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACTTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCTTCAGCCTCCCGAATAGCTGGGATTACAGGCATGTCCTATCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGCACCCGGCCTGATAATGAAATTTTTATAGATGTGTCAATGTTGTTGGAATC... | CAGAGTATCACTCTGTCACCCAGGCTGGAGTGCAGTGGTGCGATCTTGGCTCACTGCAACTTCCGCCTCCCAGGTTCAAGCAATTCTCCTGCTTCAGCCTCCCGAATAGCTGGGATTACAGGCATGTCCTATCACGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGTTTTACCATGTTGGCCAGGCTGGTCTCGAACTCCTGACCTCAGGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTATAGGCGTGAGCCACTGCACCCGGCCTGATAATGAAATTTTTATAGATGTGTCAATGTTGTTGGAATC... |
Task1_train_42155 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CCATCTTGGCCAGGCTAGTCTCGAATTCCTGACCTCGTTATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTACCCAGCCCACTCGGGAACCTTTTTTTTTTTTTTTTTTTTTTGAGATGGTCTTTCGCTCTTGTTGCCCAGGATGGAGTGCAACGGTGCAATCTTGGCTCATTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTCTGTGCCTTCGAATATAGCAAATATCCACAGGAATAGGGCAGATGGACAGATTAGTGGATACATAGATCC... | CCATCTTGGCCAGGCTAGTCTCGAATTCCTGACCTCGTTATCCACCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGCGTGAGCCACCGTACCCAGCCCACTCGGGAACCTTTTTTTTTTTTTTTTTTTTTTGAGATGGTCTTTCGCTCTTGTTGCCCAGGATGGAGTGCAACGGTGCAATCTTGGCTCATTGCAACCTCCACCTCCCGGGTTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTCTGTGCCTTCGAATATAGCAAATATCCACAGGAATAGGGCAGATGGACAGATTAGTGGATACATAGATCC... |
Task1_train_42156 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | AAGCTCAGTAGAATATCCCAATTCCTTGAACCCACCCCCACCTGCACATGCTATAGAATTGACCACCGTTTTAATTATTTATTTTCCAGAAGTTTACAACTCAACTTGCAATTTTCCCGTGTAAGATTCACTTTAGGAAATTTACTTTTGCTGATGGAGTCTATTCTATAATGTGAATAATAAATAATGATAAAACCCCCCATAGAAACAGAACATTAAAATCTGCAGAGAATGGTAATCCACTGTGCAAACCAGCCTGGATCCAACAAATCCTAAAGGTCTTCAAAGACTCTCAAGCCCTCCAGAACGTCAGTTCTCTT... | AAGCTCAGTAGAATATCCCAATTCCTTGAACCCACCCCCACCTGCACATGCTATAGAATTGACCACCGTTTTAATTATTTATTTTCCAGAAGTTTACAACTCAACTTGCAATTTTCCCGTGTAAGATTCACTTTAGGAAATTTACTTTTGCTGATGGAGTCTATTCTATAATGTGAATAATAAATAATGATAAAACCCCCCATAGAAACAGAACATTAAAATCTGCAGAGAATGGTAATCCACTGTGCAAACCAGCCTGGATCCAACAAATCCTAAAGGTCTTCAAAGACTCTCAAGCCCTCCAGAACGTCAGTTCTCTT... |
Task1_train_42157 | This is a variant located on Chromosome 12. Is this mutation a likely cause of disease or not? | Benign | ACATGCTATAGAATTGACCACCGTTTTAATTATTTATTTTCCAGAAGTTTACAACTCAACTTGCAATTTTCCCGTGTAAGATTCACTTTAGGAAATTTACTTTTGCTGATGGAGTCTATTCTATAATGTGAATAATAAATAATGATAAAACCCCCCATAGAAACAGAACATTAAAATCTGCAGAGAATGGTAATCCACTGTGCAAACCAGCCTGGATCCAACAAATCCTAAAGGTCTTCAAAGACTCTCAAGCCCTCCAGAACGTCAGTTCTCTTTTTCTTATGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGC... | ACATGCTATAGAATTGACCACCGTTTTAATTATTTATTTTCCAGAAGTTTACAACTCAACTTGCAATTTTCCCGTGTAAGATTCACTTTAGGAAATTTACTTTTGCTGATGGAGTCTATTCTATAATGTGAATAATAAATAATGATAAAACCCCCCATAGAAACAGAACATTAAAATCTGCAGAGAATGGTAATCCACTGTGCAAACCAGCCTGGATCCAACAAATCCTAAAGGTCTTCAAAGACTCTCAAGCCCTCCAGAACGTCAGTTCTCTTTTTCTTATGAGACAGAGTCTCACTCTGTCACCCAGGCTGGAGTGC... |
Task1_train_42158 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AGCCCTTCACAGAAAACACTCAGCGGAGGGGTTGGGTGGGGCAGGGGGTGGGGAGCAGCAGGAGAGGAATAAGGCCTCCCTTCTCTCAAACCCCACAGCCCACTCCCCACATTCATGCCTAGGCCTCGGCCCTGGGGAGGAAGCCCTTAGGAATACATTCTGCTTCTGACCAGGAATAGCTGGGGTTTCACTGAGGCCTCTGGGTCTTCCTCTCCCCTTCCCCGTAAGTCTCATTTTTTGAGTGTCTGGGAGAATTTGGTCCCCTGGATGGAGTGGGGGGGAGGGGGCAGGTGTGAGGGGCACACAGGAGAGCAGCCAAA... | AGCCCTTCACAGAAAACACTCAGCGGAGGGGTTGGGTGGGGCAGGGGGTGGGGAGCAGCAGGAGAGGAATAAGGCCTCCCTTCTCTCAAACCCCACAGCCCACTCCCCACATTCATGCCTAGGCCTCGGCCCTGGGGAGGAAGCCCTTAGGAATACATTCTGCTTCTGACCAGGAATAGCTGGGGTTTCACTGAGGCCTCTGGGTCTTCCTCTCCCCTTCCCCGTAAGTCTCATTTTTTGAGTGTCTGGGAGAATTTGGTCCCCTGGATGGAGTGGGGGGGAGGGGGCAGGTGTGAGGGGCACACAGGAGAGCAGCCAAA... |
Task1_train_42159 | A sequence alteration has been identified on Chromosome 12. Is it disease-inducing or harmless? | Benign | AATATTAAAGAATATTTTGATAACAATTTATCATTATATTAACAGATCATTTAATTTAAATATTTCATATTTAATTTATCACACTGAAACTAATCTATTAAATTTCATACATCATAATTTCTGGCCAATCCCTCCCTCACTACTGCCTGCCGCACTTTGTGCCCCGACTGCCCACCTGCACTAGACACATAATGTCGGTACTCACAATTTCGTTTGTTTGTTTGTTTTGTTTTTTGAGAAGGAGTTTCGCTCTTGTTGCCTAGGCTGGAGAGCAATGGTGCGATCCCGGCTTACTGCAACCTCTGCCTCCCGGGTTCAAG... | AATATTAAAGAATATTTTGATAACAATTTATCATTATATTAACAGATCATTTAATTTAAATATTTCATATTTAATTTATCACACTGAAACTAATCTATTAAATTTCATACATCATAATTTCTGGCCAATCCCTCCCTCACTACTGCCTGCCGCACTTTGTGCCCCGACTGCCCACCTGCACTAGACACATAATGTCGGTACTCACAATTTCGTTTGTTTGTTTGTTTTGTTTTTTGAGAAGGAGTTTCGCTCTTGTTGCCTAGGCTGGAGAGCAATGGTGCGATCCCGGCTTACTGCAACCTCTGCCTCCCGGGTTCAAG... |
Task1_train_42160 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | GCCCTGCCCGGGCAAGGAGACCCCCACCCCAGGCTGCAGGCTGGGGGCCCTGTATTGGGCCTGTGTCCACAATGATCCCACCCAGCTCCAAGCCATACTGGATGGTGGGGTCTCCCCAGAGGAGGCCACCCAGGTGGACAGCAATGGGAGGGTGAGATGTCCTGGCTTCCCAGAACAGCTGGGGGCATCTTTGCATCCCCACCACACCGTCCTGGCCTGGCTCCCTGAGAGGGGTTCAGGGGCAATACCTCCTGCAGTCCTAAGGAGGAAGGGAATGGTTAAGGGCGGGTCTTCACGGGGTTTGGGGCAGGCTCTGGGAC... | GCCCTGCCCGGGCAAGGAGACCCCCACCCCAGGCTGCAGGCTGGGGGCCCTGTATTGGGCCTGTGTCCACAATGATCCCACCCAGCTCCAAGCCATACTGGATGGTGGGGTCTCCCCAGAGGAGGCCACCCAGGTGGACAGCAATGGGAGGGTGAGATGTCCTGGCTTCCCAGAACAGCTGGGGGCATCTTTGCATCCCCACCACACCGTCCTGGCCTGGCTCCCTGAGAGGGGTTCAGGGGCAATACCTCCTGCAGTCCTAAGGAGGAAGGGAATGGTTAAGGGCGGGTCTTCACGGGGTTTGGGGCAGGCTCTGGGAC... |
Task1_train_42161 | This variant is found on Chromosome 12. What is the clinical effect of this variant — benign or pathogenic? State the disease if applicable. | Benign | AGCCCCACCCTTGTTGCACGGTGTTCTACACCAGACTCTGTCATGCTGGGTGGAGGGCGGTTTGGGAGCTTCATCACCCCCTTTCCTGGGGACCAAGCTTACCCTTGCTGCCCTGCAGGCCACGTGCCTCTAGTGAGTCTCCTGCTCAACTACTATGTGGGCCTGGACCTGGAACGCCGGGACCAGCGGGGGCTCACGGCGTTAATGAAGGCTGCCATGCGGAACCGCTGTGAGTGCGTGGCCACCCTCCTCATGGCAGGTGTGCGGGGCCTGGACCGGGGTGTGTGGCCTCCAGTCCCTCCTCCAAGCCTTCCCACCAG... | AGCCCCACCCTTGTTGCACGGTGTTCTACACCAGACTCTGTCATGCTGGGTGGAGGGCGGTTTGGGAGCTTCATCACCCCCTTTCCTGGGGACCAAGCTTACCCTTGCTGCCCTGCAGGCCACGTGCCTCTAGTGAGTCTCCTGCTCAACTACTATGTGGGCCTGGACCTGGAACGCCGGGACCAGCGGGGGCTCACGGCGTTAATGAAGGCTGCCATGCGGAACCGCTGTGAGTGCGTGGCCACCCTCCTCATGGCAGGTGTGCGGGGCCTGGACCGGGGTGTGTGGCCTCCAGTCCCTCCTCCAAGCCTTCCCACCAG... |
Task1_train_42162 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GGGGAACTTTTAAAAAATGCATGTTTCTTGCTGATTCCAGGACTGAATCAGAGTCTGGAGTGAGGGTGAAACCAGTGAATATGCTTTTCTCAGTGAGCACTTCAGGTGATTCTGATGCGTGATAAAGTAGAAGGAGGGTGGACTGGGGCACGGCCAGAGAAGTAGAGGTACGGACAGAGGATCCTAGAGGAATGCCGGATTTTAGCCTTATTGTTAGCCACTTTTTCCTTTCCACCTCAAACCCTCTCCTTTGCAGCTTTCTGGGCTAGCAAAGGCTGCCAAGGATGGCTTCCTGCTAGTACCCCAGTGGGCAGATTCAG... | GGGGAACTTTTAAAAAATGCATGTTTCTTGCTGATTCCAGGACTGAATCAGAGTCTGGAGTGAGGGTGAAACCAGTGAATATGCTTTTCTCAGTGAGCACTTCAGGTGATTCTGATGCGTGATAAAGTAGAAGGAGGGTGGACTGGGGCACGGCCAGAGAAGTAGAGGTACGGACAGAGGATCCTAGAGGAATGCCGGATTTTAGCCTTATTGTTAGCCACTTTTTCCTTTCCACCTCAAACCCTCTCCTTTGCAGCTTTCTGGGCTAGCAAAGGCTGCCAAGGATGGCTTCCTGCTAGTACCCCAGTGGGCAGATTCAG... |
Task1_train_42163 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TTTTACAGTTGAGGAGACGGGGGCACAGAATGACAGTGGGCTTGAGGCAGCATCAGGGTCCGAAACCGGGCAGTCTGCCCCGGGGCCAGTGCTCATCATCACTGTGTGCACTTAAACCTCTCTGGCCCTTGATTTCCTCATGCACGCAATGCATGTGAGTGCCTGCACTGCCTGCTTATTGCTGCCTGGTTGTTACTGTGGGTTGCCACAGGGGACTCTGATTTAGAGGGACTGCGACAGGTAGAGAGACCTGCCCTGGGCAGGCAGCCCTGAGGTCGATGTTCTCTCAGCCCTGGAGTGGACGGAGGATAGGTGGGTCG... | TTTTACAGTTGAGGAGACGGGGGCACAGAATGACAGTGGGCTTGAGGCAGCATCAGGGTCCGAAACCGGGCAGTCTGCCCCGGGGCCAGTGCTCATCATCACTGTGTGCACTTAAACCTCTCTGGCCCTTGATTTCCTCATGCACGCAATGCATGTGAGTGCCTGCACTGCCTGCTTATTGCTGCCTGGTTGTTACTGTGGGTTGCCACAGGGGACTCTGATTTAGAGGGACTGCGACAGGTAGAGAGACCTGCCCTGGGCAGGCAGCCCTGAGGTCGATGTTCTCTCAGCCCTGGAGTGGACGGAGGATAGGTGGGTCG... |
Task1_train_42164 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | TACTCCAAGTGAACATTTAAGATCAGTGACTTGGATGGAGACTTAAAAAGGAAGTCAGCTGACTCCGTGTAGTCATCCAGAGCTGTGAGGAATGACAAGTGCACAGTATAAAATCAAGATTCTAATTGAAGGTAACTGGGCAGAAGGATGGGCCGAGATTAACGGTGTGAATGTGACTGACGATTCCTGTGCTGAGGCCTCTGCTGGACTTAAGAAAGTCAGCTGAGGAGTTCAGGCCCTGTGCCTGGCTCAAAGGCCCAGGGACCCAGGCCCTTAGCTTCTGCCCTGCTCTCTGGATGGAGGCTGTGGGACTGCTCTGT... | TACTCCAAGTGAACATTTAAGATCAGTGACTTGGATGGAGACTTAAAAAGGAAGTCAGCTGACTCCGTGTAGTCATCCAGAGCTGTGAGGAATGACAAGTGCACAGTATAAAATCAAGATTCTAATTGAAGGTAACTGGGCAGAAGGATGGGCCGAGATTAACGGTGTGAATGTGACTGACGATTCCTGTGCTGAGGCCTCTGCTGGACTTAAGAAAGTCAGCTGAGGAGTTCAGGCCCTGTGCCTGGCTCAAAGGCCCAGGGACCCAGGCCCTTAGCTTCTGCCCTGCTCTCTGGATGGAGGCTGTGGGACTGCTCTGT... |
Task1_train_42165 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | TCCTCCTCATACCTGAGACAGAGCAGAGGGAAGAGAGGGGAGGTCAGGGCAGGGCAGGTCTCTGCAGAGCCACCATCACATCACACTTCATCACAGCCATGGGGACAGTACTAGAAACACCTCCACACAGCCCCGGCCTGGCAGCCTAGCTTAGTGCTTTCTAGTTGGATGTGGGATGTGTCTGGGATTCTCTATCCACTTTGAACTGGGGATGGAGAGTGCTCATCTGGGACCTCCCAGTCCTGTTCCCAAAGGGGCTCTGAGGTCCCCCAGGAGGCAAATAGGACTCAGCCCCCAGCCCCATCCTGGGAGTGGACAGC... | TCCTCCTCATACCTGAGACAGAGCAGAGGGAAGAGAGGGGAGGTCAGGGCAGGGCAGGTCTCTGCAGAGCCACCATCACATCACACTTCATCACAGCCATGGGGACAGTACTAGAAACACCTCCACACAGCCCCGGCCTGGCAGCCTAGCTTAGTGCTTTCTAGTTGGATGTGGGATGTGTCTGGGATTCTCTATCCACTTTGAACTGGGGATGGAGAGTGCTCATCTGGGACCTCCCAGTCCTGTTCCCAAAGGGGCTCTGAGGTCCCCCAGGAGGCAAATAGGACTCAGCCCCCAGCCCCATCCTGGGAGTGGACAGC... |
Task1_train_42166 | A mutation on Chromosome 12 is under review. Please evaluate whether this mutation is benign or pathogenic and specify the disease if necessary. | Benign | CACCTCCACACAGCCCCGGCCTGGCAGCCTAGCTTAGTGCTTTCTAGTTGGATGTGGGATGTGTCTGGGATTCTCTATCCACTTTGAACTGGGGATGGAGAGTGCTCATCTGGGACCTCCCAGTCCTGTTCCCAAAGGGGCTCTGAGGTCCCCCAGGAGGCAAATAGGACTCAGCCCCCAGCCCCATCCTGGGAGTGGACAGCGTGGACTCTCAGGGCCTGTAGCCCTAGCCTCCCCTCACTGGTATCAATCCCAGCTCAGGTATGGGGCCTCCTGGACCCGCAGACCCTCAGGACTTAGAACCTAAGGCAGTGGGACAC... | CACCTCCACACAGCCCCGGCCTGGCAGCCTAGCTTAGTGCTTTCTAGTTGGATGTGGGATGTGTCTGGGATTCTCTATCCACTTTGAACTGGGGATGGAGAGTGCTCATCTGGGACCTCCCAGTCCTGTTCCCAAAGGGGCTCTGAGGTCCCCCAGGAGGCAAATAGGACTCAGCCCCCAGCCCCATCCTGGGAGTGGACAGCGTGGACTCTCAGGGCCTGTAGCCCTAGCCTCCCCTCACTGGTATCAATCCCAGCTCAGGTATGGGGCCTCCTGGACCCGCAGACCCTCAGGACTTAGAACCTAAGGCAGTGGGACAC... |
Task1_train_42167 | A genetic alteration is present on Chromosome 12. Is this variant benign or disease-causing, and if the latter, which condition is involved? | Benign | ACTTGCTATTGAGTTGTTTGAGTTCCTTATATATTGCAGCTACGAATTCCTTGTCAGTTGAATAGTTTGCAAATATTTCTTCCATTCTGTAGGTCATTTCTTCAACTTGTTGATTGTTTCCTTTGGTGTGCAGAAGTTCTTTTAGCTCGATGTGATCCCATTTGCCCATTTTTTGCTTTGGTTGCCTTTGGTTTTGAGGTCTCAATCAAGAAATCTTTGTCCAGGTCAATGCCCTAAGCATTTCCTCAATGTTTTCTTCTAGTAGTTTCATAGTCTGAGGTCTTATATTTAAGTCTTTAATCCATTTTAATTTGGTTTTT... | ACTTGCTATTGAGTTGTTTGAGTTCCTTATATATTGCAGCTACGAATTCCTTGTCAGTTGAATAGTTTGCAAATATTTCTTCCATTCTGTAGGTCATTTCTTCAACTTGTTGATTGTTTCCTTTGGTGTGCAGAAGTTCTTTTAGCTCGATGTGATCCCATTTGCCCATTTTTTGCTTTGGTTGCCTTTGGTTTTGAGGTCTCAATCAAGAAATCTTTGTCCAGGTCAATGCCCTAAGCATTTCCTCAATGTTTTCTTCTAGTAGTTTCATAGTCTGAGGTCTTATATTTAAGTCTTTAATCCATTTTAATTTGGTTTTT... |
Task1_train_42168 | Here is a variant on Chromosome 12. Please identify whether it is a benign mutation or associated with a disorder. | Benign | ACTGAAAGCTCAGCCTTGTGTATGATGAAGGTCTCTGGCTGCTGTGAGGTGGGGCATGGAAGGGAGAAGAGCAGGACTCCAGGCAAAATGGTGATGGCTGGGTGTGCTGGCAGCAGTAAGGAGAGAGGAAAGAGGGGGATGGAGAGCTATTTAGGAGGCAGAAAAAGAAGTCCTTGGGTTTAGTGAATATTGAGGGCGCAGGCATGGATAAATCATAGGTTCTGGTTTGGGCAACTGTGTTGATGATCTTGGCAGGAGAGACTGGAGGAGACTCCGGTTGAGAGGGTGGGAAGCAATGAGTTAAGCTGGAAGGTATGCTG... | ACTGAAAGCTCAGCCTTGTGTATGATGAAGGTCTCTGGCTGCTGTGAGGTGGGGCATGGAAGGGAGAAGAGCAGGACTCCAGGCAAAATGGTGATGGCTGGGTGTGCTGGCAGCAGTAAGGAGAGAGGAAAGAGGGGGATGGAGAGCTATTTAGGAGGCAGAAAAAGAAGTCCTTGGGTTTAGTGAATATTGAGGGCGCAGGCATGGATAAATCATAGGTTCTGGTTTGGGCAACTGTGTTGATGATCTTGGCAGGAGAGACTGGAGGAGACTCCGGTTGAGAGGGTGGGAAGCAATGAGTTAAGCTGGAAGGTATGCTG... |
Task1_train_42169 | Given this variant on Chromosome 12, classify it as benign or pathogenic. Include the disorder it may cause if applicable. | Benign | CCAGATGCTTTCCAGGGGCTCAGACCCTGTATGGGGGGCCTCTTTCCATTCTCCTAGACCAACCCCATGTAGGAAGGCTATTGCTGCCAGAGAAAGCCCTGGGCCAGAGCAATGGGTTCAATTCTGTTTGATGCTGTGTGGGGTCTATGCTGCAGTCCACTGGCTCAGGGGAAGGATGCAGGGCAGGTTCCCAAGGCACAGGTGTCTGGGGTGCTCACTCTCCTGCCCCTTACTAAATTTGTTCCTTTTTGGCTTTCCATCCGTTTGCCTCCCTGTTCCTTCCCTCTCCTTGCTCCCTGCCAACCCTCCAGCCGTGAGCC... | CCAGATGCTTTCCAGGGGCTCAGACCCTGTATGGGGGGCCTCTTTCCATTCTCCTAGACCAACCCCATGTAGGAAGGCTATTGCTGCCAGAGAAAGCCCTGGGCCAGAGCAATGGGTTCAATTCTGTTTGATGCTGTGTGGGGTCTATGCTGCAGTCCACTGGCTCAGGGGAAGGATGCAGGGCAGGTTCCCAAGGCACAGGTGTCTGGGGTGCTCACTCTCCTGCCCCTTACTAAATTTGTTCCTTTTTGGCTTTCCATCCGTTTGCCTCCCTGTTCCTTCCCTCTCCTTGCTCCCTGCCAACCCTCCAGCCGTGAGCC... |
Task1_train_42170 | A variant was discovered on Chromosome 12. What is its functional impact — neutral or pathogenic? State the disease if pathogenic. | Benign | CCATACAGTCTTCCCTGTGATCCTGTCTCTGACCCTCGCCAGGCAGTCGTGAGCTGCTTCTTGGGGCTCCCATGCTGTTTGGCCCTCATTATTTATGAATCTTCTCTCCGGGAGGCTGAGCGTCCTTCCAAGGTTAAGAGGGAGTCTTAGTCAATTCTGCAGCACCAGCCTCTAATGCAGGGCTTGGCGCAGCATGGGTGCTCTTTGGGGAGAGTGGGGAGTCATCCCAACTCTCAGGAGAGGGGAGCCATAAGGGGGAAAGCACCCCCCAGGAGGGGCTGTTTCAGGGGGTCGGTGAGGCAGAGGAAAGGGGACTGAGG... | CCATACAGTCTTCCCTGTGATCCTGTCTCTGACCCTCGCCAGGCAGTCGTGAGCTGCTTCTTGGGGCTCCCATGCTGTTTGGCCCTCATTATTTATGAATCTTCTCTCCGGGAGGCTGAGCGTCCTTCCAAGGTTAAGAGGGAGTCTTAGTCAATTCTGCAGCACCAGCCTCTAATGCAGGGCTTGGCGCAGCATGGGTGCTCTTTGGGGAGAGTGGGGAGTCATCCCAACTCTCAGGAGAGGGGAGCCATAAGGGGGAAAGCACCCCCCAGGAGGGGCTGTTTCAGGGGGTCGGTGAGGCAGAGGAAAGGGGACTGAGG... |
Task1_train_42171 | A genomic change on Chromosome 12 is noted. Classify this variant as benign or pathogenic, and name the disease if relevant. | Benign | TGATCCTGTCTCTGACCCTCGCCAGGCAGTCGTGAGCTGCTTCTTGGGGCTCCCATGCTGTTTGGCCCTCATTATTTATGAATCTTCTCTCCGGGAGGCTGAGCGTCCTTCCAAGGTTAAGAGGGAGTCTTAGTCAATTCTGCAGCACCAGCCTCTAATGCAGGGCTTGGCGCAGCATGGGTGCTCTTTGGGGAGAGTGGGGAGTCATCCCAACTCTCAGGAGAGGGGAGCCATAAGGGGGAAAGCACCCCCCAGGAGGGGCTGTTTCAGGGGGTCGGTGAGGCAGAGGAAAGGGGACTGAGGCCTCACAGAGGGTGGAA... | TGATCCTGTCTCTGACCCTCGCCAGGCAGTCGTGAGCTGCTTCTTGGGGCTCCCATGCTGTTTGGCCCTCATTATTTATGAATCTTCTCTCCGGGAGGCTGAGCGTCCTTCCAAGGTTAAGAGGGAGTCTTAGTCAATTCTGCAGCACCAGCCTCTAATGCAGGGCTTGGCGCAGCATGGGTGCTCTTTGGGGAGAGTGGGGAGTCATCCCAACTCTCAGGAGAGGGGAGCCATAAGGGGGAAAGCACCCCCCAGGAGGGGCTGTTTCAGGGGGTCGGTGAGGCAGAGGAAAGGGGACTGAGGCCTCACAGAGGGTGGAA... |
Task1_train_42172 | Chromosome 12 houses a mutation. Classify its clinical impact — is it pathogenic or benign, and what disease does it lead to if any? | Benign | ATGGGTAATTACGGAGAACTGGGGGCTTGAATTCCCTGAGCTCACAGAAACCCAAGTAGGGCTAATGGGGCCATCAACGTAGAGGGAACATGTTGGGAGGTTTGAACTCTGCAGATATTCTCAAGGTTGATGTGACATTTCTTGGGTGGCCCAAGGGTCAGAGGTCAGGTTACCCCACACTCCAGATTCCATTTTAAACCTTCTCCTTTGAGAGAAACATCCCCACTCACCTTTTTCAGGGCTACAAATTCATTCTCAGCAGCTGTGCGCTTGTTAATTTCATCTTCGTACCTATAAGGACAGAGCGGGGGGTGTGCTGT... | ATGGGTAATTACGGAGAACTGGGGGCTTGAATTCCCTGAGCTCACAGAAACCCAAGTAGGGCTAATGGGGCCATCAACGTAGAGGGAACATGTTGGGAGGTTTGAACTCTGCAGATATTCTCAAGGTTGATGTGACATTTCTTGGGTGGCCCAAGGGTCAGAGGTCAGGTTACCCCACACTCCAGATTCCATTTTAAACCTTCTCCTTTGAGAGAAACATCCCCACTCACCTTTTTCAGGGCTACAAATTCATTCTCAGCAGCTGTGCGCTTGTTAATTTCATCTTCGTACCTATAAGGACAGAGCGGGGGGTGTGCTGT... |
Task1_train_42173 | Located on Chromosome 12, this mutation has been observed. What is its biological consequence — is it benign or pathogenic, and which disease is associated if any? | Benign | TGACATTTCTTGGGTGGCCCAAGGGTCAGAGGTCAGGTTACCCCACACTCCAGATTCCATTTTAAACCTTCTCCTTTGAGAGAAACATCCCCACTCACCTTTTTCAGGGCTACAAATTCATTCTCAGCAGCTGTGCGCTTGTTAATTTCATCTTCGTACCTATAAGGACAGAGCGGGGGGTGTGCTGTTGAGCAAGTCTGCATTGAACTCTTTCCAGGCTGGTGTAGCAAGAGTTAAGAGCCCTCAAATCATTTCCAGCTCTTCTGCTGACCTGGGCATGACTTTGGGTGATTCATTTAACCTCTATTTCTCCCTCCATA... | TGACATTTCTTGGGTGGCCCAAGGGTCAGAGGTCAGGTTACCCCACACTCCAGATTCCATTTTAAACCTTCTCCTTTGAGAGAAACATCCCCACTCACCTTTTTCAGGGCTACAAATTCATTCTCAGCAGCTGTGCGCTTGTTAATTTCATCTTCGTACCTATAAGGACAGAGCGGGGGGTGTGCTGTTGAGCAAGTCTGCATTGAACTCTTTCCAGGCTGGTGTAGCAAGAGTTAAGAGCCCTCAAATCATTTCCAGCTCTTCTGCTGACCTGGGCATGACTTTGGGTGATTCATTTAACCTCTATTTCTCCCTCCATA... |
Task1_train_42174 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TATAGGTCATTTTCTTCTCAGAATTATGGCAGACTCAGATACCTGTAATAATACGGGAACTAAAAAGGACATTCGCATGTCTGAGTGCTGATAACTGTTGACTTGATGGTAAGCAACAGGAGCTCAGTGGAACAGGTATTGATGAGAAGAAAAGTGAGGGCATCCCAGCTCTACCCGGGAGGGCAGGGGAGACTGGAGGCCAGGGGAGGACAAGCAACCTGAGGAGAGGGCTCTGCTGCCAGAGAGGGGCCTGAGAGCTGTGGGACTGAGAGCTGGCGGCAGCACTTCAGTGCTTGTAGCTCTTCCTGCTGGAGGAGGAG... | TATAGGTCATTTTCTTCTCAGAATTATGGCAGACTCAGATACCTGTAATAATACGGGAACTAAAAAGGACATTCGCATGTCTGAGTGCTGATAACTGTTGACTTGATGGTAAGCAACAGGAGCTCAGTGGAACAGGTATTGATGAGAAGAAAAGTGAGGGCATCCCAGCTCTACCCGGGAGGGCAGGGGAGACTGGAGGCCAGGGGAGGACAAGCAACCTGAGGAGAGGGCTCTGCTGCCAGAGAGGGGCCTGAGAGCTGTGGGACTGAGAGCTGGCGGCAGCACTTCAGTGCTTGTAGCTCTTCCTGCTGGAGGAGGAG... |
Task1_train_42175 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | TTCACTGACCATCCACTTATATCCTGAGACTTTCCTTAGCCATTCAGAGATGCCAGCCCAGTTCACAGACAGGCCAGTTCACTCCTGAGGGAGGAATATAACTGTCTCTTCCGGTAAACAGACTCGGTTTTGTGGGATCTCTGAGAGGCTTAGAGTGTGAAAGGGAGGGAATTTCCATGCTTGTTTTGCTTTTGCATTTCAAGGAATAAGCATGAGAGTTTTGTGCCTGGCTGTTTGGATTTTTATTTTTTATTTTTCGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTAGTGTGATCTCAGCTCACTGCA... | TTCACTGACCATCCACTTATATCCTGAGACTTTCCTTAGCCATTCAGAGATGCCAGCCCAGTTCACAGACAGGCCAGTTCACTCCTGAGGGAGGAATATAACTGTCTCTTCCGGTAAACAGACTCGGTTTTGTGGGATCTCTGAGAGGCTTAGAGTGTGAAAGGGAGGGAATTTCCATGCTTGTTTTGCTTTTGCATTTCAAGGAATAAGCATGAGAGTTTTGTGCCTGGCTGTTTGGATTTTTATTTTTTATTTTTCGAGATGGAGTCTTGCTCTGTTGCCCAGGCTGGAGTGCAGTAGTGTGATCTCAGCTCACTGCA... |
Task1_train_42176 | A variant found on Chromosome 12 is being studied. Please analyze its biological impact: is it benign or pathogenic, and what condition might it cause? | Benign | GAGGTTGAATCAGTAATAAAAAGTATTCCAACAAAGAAAAATCTAGGAGCAGATAACCTTACTACTGAATTCTACTCAACATGTACAGAAGAATTAGTAACAATTCTTCTCAAACTAAGCTATCAAATTTCCAATAGAGTTGTTTGTAGTATTTCTTTGTTACATTTTTAATGCCCATGAACCATAAGATTTTAATTTTATTTAAACCTATATGGATAATTTTTAACCTCCTTTTGCTGTATTGTTATATTCTAGATAATTTTTCTTATCAATTATTTTCTTTTTCATTATTTCTCAAGGGTACATATATATGCGGTAAG... | GAGGTTGAATCAGTAATAAAAAGTATTCCAACAAAGAAAAATCTAGGAGCAGATAACCTTACTACTGAATTCTACTCAACATGTACAGAAGAATTAGTAACAATTCTTCTCAAACTAAGCTATCAAATTTCCAATAGAGTTGTTTGTAGTATTTCTTTGTTACATTTTTAATGCCCATGAACCATAAGATTTTAATTTTATTTAAACCTATATGGATAATTTTTAACCTCCTTTTGCTGTATTGTTATATTCTAGATAATTTTTCTTATCAATTATTTTCTTTTTCATTATTTCTCAAGGGTACATATATATGCGGTAAG... |
Task1_train_42177 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | AATGAATTTGAACCCCCGGCTTCATCTGCTCACCTTCTTCAGAGTCACAAATTCATTCTCTGCTGCTGTGCGCTTGTTGATTTCATCCTCATATCTACAGGAAGAAAGGCATGGGACACATTTGAGCCAGTGGGTAGGATGAAACAGAAAAGCAGCCTGGGATTCAACATTTTCCCGAATGGAATATATTCTAATTGGGCTTTCCTGCCACAGAGAGCCTAAGAGACGATTTTTGCTTCTGCTAAATTTGCCACTTCTTTAATCTCCCCATCCTCCCATAACCATCTGTGGTTCTTGCAGGTTTGCTCCTAGGGACTAAT... | AATGAATTTGAACCCCCGGCTTCATCTGCTCACCTTCTTCAGAGTCACAAATTCATTCTCTGCTGCTGTGCGCTTGTTGATTTCATCCTCATATCTACAGGAAGAAAGGCATGGGACACATTTGAGCCAGTGGGTAGGATGAAACAGAAAAGCAGCCTGGGATTCAACATTTTCCCGAATGGAATATATTCTAATTGGGCTTTCCTGCCACAGAGAGCCTAAGAGACGATTTTTGCTTCTGCTAAATTTGCCACTTCTTTAATCTCCCCATCCTCCCATAACCATCTGTGGTTCTTGCAGGTTTGCTCCTAGGGACTAAT... |
Task1_train_42178 | A mutation on Chromosome 12 has been found. Is it harmful or harmless? What disease, if any, does it cause? | Benign | ATACAATTGGAAATCCAAAATTGGCTAAAATAATTTATACATCTAAAAGATAAAAAGGTGTGCAGGCTGTCTTGGTGTCTCCACCACATAAATTCTGAATTTACTTTCACATTTGCTGACATACAATAATTGACAATTCTTCATGGTCTTAATCCATACTGAAGCTCAAATAATACTTATACCTGGGGATCCTATTAAATTTAAACAAGGTACCCCTGTAATCTTGGGGAAGTTAATGAACAAAAAATAGAGAACAAACAGGCATGCCTCACTTTAATTAGCAGAACTACTGACTTGCTTAAATTTCCCACGATCATAGC... | ATACAATTGGAAATCCAAAATTGGCTAAAATAATTTATACATCTAAAAGATAAAAAGGTGTGCAGGCTGTCTTGGTGTCTCCACCACATAAATTCTGAATTTACTTTCACATTTGCTGACATACAATAATTGACAATTCTTCATGGTCTTAATCCATACTGAAGCTCAAATAATACTTATACCTGGGGATCCTATTAAATTTAAACAAGGTACCCCTGTAATCTTGGGGAAGTTAATGAACAAAAAATAGAGAACAAACAGGCATGCCTCACTTTAATTAGCAGAACTACTGACTTGCTTAAATTTCCCACGATCATAGC... |
Task1_train_42179 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | AAAGATAAAAAGGTGTGCAGGCTGTCTTGGTGTCTCCACCACATAAATTCTGAATTTACTTTCACATTTGCTGACATACAATAATTGACAATTCTTCATGGTCTTAATCCATACTGAAGCTCAAATAATACTTATACCTGGGGATCCTATTAAATTTAAACAAGGTACCCCTGTAATCTTGGGGAAGTTAATGAACAAAAAATAGAGAACAAACAGGCATGCCTCACTTTAATTAGCAGAACTACTGACTTGCTTAAATTTCCCACGATCATAGCATCCTCTAACGTTTCCCACAATGGGCATGGACAGTCTAACCCAAT... | AAAGATAAAAAGGTGTGCAGGCTGTCTTGGTGTCTCCACCACATAAATTCTGAATTTACTTTCACATTTGCTGACATACAATAATTGACAATTCTTCATGGTCTTAATCCATACTGAAGCTCAAATAATACTTATACCTGGGGATCCTATTAAATTTAAACAAGGTACCCCTGTAATCTTGGGGAAGTTAATGAACAAAAAATAGAGAACAAACAGGCATGCCTCACTTTAATTAGCAGAACTACTGACTTGCTTAAATTTCCCACGATCATAGCATCCTCTAACGTTTCCCACAATGGGCATGGACAGTCTAACCCAAT... |
Task1_train_42180 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | AATAAAACAAAGTAGGTGTTTCTTTTAGAACTCAGGCCCCTTCCTTGCCCTCTTTCAATCTCACCCTACCTGTTTCTTGACATTGTCAATCTCGGCTCTCAGCCTCTGGATCATCCGGTTCATCTCAGAGATCTCATGCTTGGTGTTGCGGAGGTCATCGCCATGCCGGCCAGCTGTCTGCTGCAGCTCCTCATACTGATGCAGCCAGGAAAGAGGAAAGATTCTGTTTATATGAGAATGGGAAGAACTTTCCCAAAGTTCACAGGCAGTGAGTACTAAGTGGTGGCAAATAGTGTGGGGCTGGTTCAGGCTTTTCCAAG... | AATAAAACAAAGTAGGTGTTTCTTTTAGAACTCAGGCCCCTTCCTTGCCCTCTTTCAATCTCACCCTACCTGTTTCTTGACATTGTCAATCTCGGCTCTCAGCCTCTGGATCATCCGGTTCATCTCAGAGATCTCATGCTTGGTGTTGCGGAGGTCATCGCCATGCCGGCCAGCTGTCTGCTGCAGCTCCTCATACTGATGCAGCCAGGAAAGAGGAAAGATTCTGTTTATATGAGAATGGGAAGAACTTTCCCAAAGTTCACAGGCAGTGAGTACTAAGTGGTGGCAAATAGTGTGGGGCTGGTTCAGGCTTTTCCAAG... |
Task1_train_42181 | Here is a genetic alteration on Chromosome 12. Based on the data, is it a benign variant or a cause of disease? | Benign | CTTCCTTGCCCTCTTTCAATCTCACCCTACCTGTTTCTTGACATTGTCAATCTCGGCTCTCAGCCTCTGGATCATCCGGTTCATCTCAGAGATCTCATGCTTGGTGTTGCGGAGGTCATCGCCATGCCGGCCAGCTGTCTGCTGCAGCTCCTCATACTGATGCAGCCAGGAAAGAGGAAAGATTCTGTTTATATGAGAATGGGAAGAACTTTCCCAAAGTTCACAGGCAGTGAGTACTAAGTGGTGGCAAATAGTGTGGGGCTGGTTCAGGCTTTTCCAAGGCTGAGCTAGTCTAGTGCCTTTGCTCTCCTGGAGACACT... | CTTCCTTGCCCTCTTTCAATCTCACCCTACCTGTTTCTTGACATTGTCAATCTCGGCTCTCAGCCTCTGGATCATCCGGTTCATCTCAGAGATCTCATGCTTGGTGTTGCGGAGGTCATCGCCATGCCGGCCAGCTGTCTGCTGCAGCTCCTCATACTGATGCAGCCAGGAAAGAGGAAAGATTCTGTTTATATGAGAATGGGAAGAACTTTCCCAAAGTTCACAGGCAGTGAGTACTAAGTGGTGGCAAATAGTGTGGGGCTGGTTCAGGCTTTTCCAAGGCTGAGCTAGTCTAGTGCCTTTGCTCTCCTGGAGACACT... |
Task1_train_42182 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TGATATGACAACTTGAGGAAAAAAAACCCACCCATGTGAAAAATTTAGATAAGTTTCTTACCGCATCAAAGAACATCTTCATGAAGTTAATCTCATCCATCAGTGCATCAACCTTGGCCTCCAGCTCCACCTTGTTCATGTAGGCAGCATCTACATCCTGGGGAAACAGGGATGATTGGCACTGCACACACCGTCACCCTACTCAAGTGAGCTCCACGCTTAGAGAGCATAGCTGCAGGCTGCTGGTTCTCTCCCACCCACACGCACCTTCTTCAGCATCACAAACTCATTCTCAGCAGTGGTACGCTTGTTGATTTCAT... | TGATATGACAACTTGAGGAAAAAAAACCCACCCATGTGAAAAATTTAGATAAGTTTCTTACCGCATCAAAGAACATCTTCATGAAGTTAATCTCATCCATCAGTGCATCAACCTTGGCCTCCAGCTCCACCTTGTTCATGTAGGCAGCATCTACATCCTGGGGAAACAGGGATGATTGGCACTGCACACACCGTCACCCTACTCAAGTGAGCTCCACGCTTAGAGAGCATAGCTGCAGGCTGCTGGTTCTCTCCCACCCACACGCACCTTCTTCAGCATCACAAACTCATTCTCAGCAGTGGTACGCTTGTTGATTTCAT... |
Task1_train_42183 | Given a variant located on Chromosome 12, assess whether it is benign or pathogenic. Indicate the associated disease if pathogenic. | Benign | TCCCTCCTCAAATCTGTGAGATAAACCAGCATCATCTAGAGAAGCCTCCACCTTCACATTTGAGAATCTAGCCATTTCTTTTAGCCTCTCAACTGGAAAGTTCTTTCTGCTATCCAACCTCGGTCCCTACTGTTGCAAAGGCAGGAGGCTAGCAAAGGCAGCAGGTGTGCATGGTGCCTTCACTGAGGAAATGGCAATGTCTGTGCCCAGTACTGAACACACACACACACACACACACATGCATGCACACACACACATGCCTCATCTTATCAATCAAGGACGCAAACATGTTGTTGAGTCTTATTCCACTTACCCACCTG... | TCCCTCCTCAAATCTGTGAGATAAACCAGCATCATCTAGAGAAGCCTCCACCTTCACATTTGAGAATCTAGCCATTTCTTTTAGCCTCTCAACTGGAAAGTTCTTTCTGCTATCCAACCTCGGTCCCTACTGTTGCAAAGGCAGGAGGCTAGCAAAGGCAGCAGGTGTGCATGGTGCCTTCACTGAGGAAATGGCAATGTCTGTGCCCAGTACTGAACACACACACACACACACACACATGCATGCACACACACACATGCCTCATCTTATCAATCAAGGACGCAAACATGTTGTTGAGTCTTATTCCACTTACCCACCTG... |
Task1_train_42184 | Here is a genetic alteration on Chromosome 12. Based on the data, is it a benign variant or a cause of disease? | Benign | CTTCACTGAGGAAATGGCAATGTCTGTGCCCAGTACTGAACACACACACACACACACACACATGCATGCACACACACACATGCCTCATCTTATCAATCAAGGACGCAAACATGTTGTTGAGTCTTATTCCACTTACCCACCTGCTAGATGACGGTGCTGACAGGTTGATGACAGCCAGGAGTCTCCGGCTCTGACCATCTCCTGGGCAGGGGCTTTTGAGCCTTGCCCTAAGCCCCAGTCACTACTCTAAATGTCCTAGATGTCAACTCAGACCATCCGTCCCTTCCTCCGGACCCTCTGTCTTCCTCTTCCATTATACT... | CTTCACTGAGGAAATGGCAATGTCTGTGCCCAGTACTGAACACACACACACACACACACACATGCATGCACACACACACATGCCTCATCTTATCAATCAAGGACGCAAACATGTTGTTGAGTCTTATTCCACTTACCCACCTGCTAGATGACGGTGCTGACAGGTTGATGACAGCCAGGAGTCTCCGGCTCTGACCATCTCCTGGGCAGGGGCTTTTGAGCCTTGCCCTAAGCCCCAGTCACTACTCTAAATGTCCTAGATGTCAACTCAGACCATCCGTCCCTTCCTCCGGACCCTCTGTCTTCCTCTTCCATTATACT... |
Task1_train_42185 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GGCTTCTAGGTATTTTAAATGCCTGGAGCAGGCACCAGCTTCATCTTTGCTTATAGCCCCTCCTCTCCCTCCTTGGTCCTGCTCCCCAGAACCATCTTCTCTGCAACAAGCATGGCACATGGAACATGATGGACAGATGGAGCTCCTGATCCCATTGTAGCCCCTCACTGAGGCAGGAAACTGGCCAGAAGGAGATGTCCATACACACCTCTTGTTTGGTTTTTGGGGATGGGGAGCACAGTTTTTAAAATGTGACTTCCCTTAATCTACATGAGCACAGCTACTGCTTGAATAAGGTTGTCTTCCCCAACATCAGAAAC... | GGCTTCTAGGTATTTTAAATGCCTGGAGCAGGCACCAGCTTCATCTTTGCTTATAGCCCCTCCTCTCCCTCCTTGGTCCTGCTCCCCAGAACCATCTTCTCTGCAACAAGCATGGCACATGGAACATGATGGACAGATGGAGCTCCTGATCCCATTGTAGCCCCTCACTGAGGCAGGAAACTGGCCAGAAGGAGATGTCCATACACACCTCTTGTTTGGTTTTTGGGGATGGGGAGCACAGTTTTTAAAATGTGACTTCCCTTAATCTACATGAGCACAGCTACTGCTTGAATAAGGTTGTCTTCCCCAACATCAGAAAC... |
Task1_train_42186 | This sequence variant lies on Chromosome 12. Is it clinically significant, and what condition might it cause if any? | Benign | GAGGAACAGGCAGTTCGTGGATGGAGGAAAGAAGTGAGGGATCCTCTCTGTTGCATATATTCAATCCATACCAGTTTCATGATTTATCTTTGATAACAAGCTCTGCTAAGAATTCCTTTTTTCCTTGAAGCCTTGGTTGGAACCTTTCTTTCATTCAGCATGCCCACAAAAGTATTCCTCACATTCACTGTGCAGGTGACCCCTCCCAGGAAGCGAAGGGCTGCTGTGGGAGGAGACCCATTCGGTGACCACCTTGGTCTGGTACAGGGCCTCGGCCTCGGCCTTGCTCTTCAGGGCGATCTCCTCATAATGCATGCGGA... | GAGGAACAGGCAGTTCGTGGATGGAGGAAAGAAGTGAGGGATCCTCTCTGTTGCATATATTCAATCCATACCAGTTTCATGATTTATCTTTGATAACAAGCTCTGCTAAGAATTCCTTTTTTCCTTGAAGCCTTGGTTGGAACCTTTCTTTCATTCAGCATGCCCACAAAAGTATTCCTCACATTCACTGTGCAGGTGACCCCTCCCAGGAAGCGAAGGGCTGCTGTGGGAGGAGACCCATTCGGTGACCACCTTGGTCTGGTACAGGGCCTCGGCCTCGGCCTTGCTCTTCAGGGCGATCTCCTCATAATGCATGCGGA... |
Task1_train_42187 | This variant lies on Chromosome 12. Based on this context, is the mutation pathogenic or benign? If pathogenic, what disease does it cause? | Benign | ACCTTTCTTTCATTCAGCATGCCCACAAAAGTATTCCTCACATTCACTGTGCAGGTGACCCCTCCCAGGAAGCGAAGGGCTGCTGTGGGAGGAGACCCATTCGGTGACCACCTTGGTCTGGTACAGGGCCTCGGCCTCGGCCTTGCTCTTCAGGGCGATCTCCTCATAATGCATGCGGACCTCAGCGATGATGCTGTCAAGGTCCAGGTCCCGGTTGTTGTCCATGGACAGGATGACAGAGGTCTCACTGGCGTGAGTCTGGATCTGAGCGATCTCCTGCATTGAGAGAGGAAGACAGATTCAGCAACCCCCTGGCTTCC... | ACCTTTCTTTCATTCAGCATGCCCACAAAAGTATTCCTCACATTCACTGTGCAGGTGACCCCTCCCAGGAAGCGAAGGGCTGCTGTGGGAGGAGACCCATTCGGTGACCACCTTGGTCTGGTACAGGGCCTCGGCCTCGGCCTTGCTCTTCAGGGCGATCTCCTCATAATGCATGCGGACCTCAGCGATGATGCTGTCAAGGTCCAGGTCCCGGTTGTTGTCCATGGACAGGATGACAGAGGTCTCACTGGCGTGAGTCTGGATCTGAGCGATCTCCTGCATTGAGAGAGGAAGACAGATTCAGCAACCCCCTGGCTTCC... |
Task1_train_42188 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | CACATTCACTGTGCAGGTGACCCCTCCCAGGAAGCGAAGGGCTGCTGTGGGAGGAGACCCATTCGGTGACCACCTTGGTCTGGTACAGGGCCTCGGCCTCGGCCTTGCTCTTCAGGGCGATCTCCTCATAATGCATGCGGACCTCAGCGATGATGCTGTCAAGGTCCAGGTCCCGGTTGTTGTCCATGGACAGGATGACAGAGGTCTCACTGGCGTGAGTCTGGATCTGAGCGATCTCCTGCATTGAGAGAGGAAGACAGATTCAGCAACCCCCTGGCTTCCCTCTTCTGCCCCATCAGTCTTCTGGGCCCATGGTCCCT... | CACATTCACTGTGCAGGTGACCCCTCCCAGGAAGCGAAGGGCTGCTGTGGGAGGAGACCCATTCGGTGACCACCTTGGTCTGGTACAGGGCCTCGGCCTCGGCCTTGCTCTTCAGGGCGATCTCCTCATAATGCATGCGGACCTCAGCGATGATGCTGTCAAGGTCCAGGTCCCGGTTGTTGTCCATGGACAGGATGACAGAGGTCTCACTGGCGTGAGTCTGGATCTGAGCGATCTCCTGCATTGAGAGAGGAAGACAGATTCAGCAACCCCCTGGCTTCCCTCTTCTGCCCCATCAGTCTTCTGGGCCCATGGTCCCT... |
Task1_train_42189 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | AGAGAGCTCCTGACTGGACTCCTTGCATCGAAGCATCACACCTTGAGGACAACAGGGAGAGGAAATGGGGTTGGGACTGTAGTGACAGACAAAGCATTTCTTGACTTGGAAAGGGAGCCCAGGGAAGGAGAGGGAGGAGACGGGTGAGTTGGGAAGCCTTCTGCTCACAGAGCCAACCACTTGTCCATCATCTGGAGGCCTTTTTGGTGGCACAGCTGCTCCCCGAGGTTTTGGCAAGGGGATCCTTGAGCTCACTGCCACAGCTGCCTTTGGTCTTGACGTCTGCAGCTGCAGTTTTGTAGCTATAACTGCTTGAGGCG... | AGAGAGCTCCTGACTGGACTCCTTGCATCGAAGCATCACACCTTGAGGACAACAGGGAGAGGAAATGGGGTTGGGACTGTAGTGACAGACAAAGCATTTCTTGACTTGGAAAGGGAGCCCAGGGAAGGAGAGGGAGGAGACGGGTGAGTTGGGAAGCCTTCTGCTCACAGAGCCAACCACTTGTCCATCATCTGGAGGCCTTTTTGGTGGCACAGCTGCTCCCCGAGGTTTTGGCAAGGGGATCCTTGAGCTCACTGCCACAGCTGCCTTTGGTCTTGACGTCTGCAGCTGCAGTTTTGTAGCTATAACTGCTTGAGGCG... |
Task1_train_42190 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | AAGGTAAAAGTTATGATTTTTAAAGCAGAGCCCATTCATTGGCTTTTTAGATGAAGGGTGATGGGCGCTAACCTGCTGCAGCACCTGGATGCAATTGGGTACATCTCAATGAGTGATGTGGCTATTACAATTTTAAATGGGAACACACATAATACGTTTGAAATTACACCCTTTGAAACTACTTACACTTATGATTAAAAGGTTGTAGTTTCAATTTTTTAACTGTGAAATGTTTTAATTGTGAAGAGTTTTTTAAAATCATTTTAGAGAGCCTATGAGAAAAGCTTCAGCGTATACAATGATGCTTAAGACATATACAC... | AAGGTAAAAGTTATGATTTTTAAAGCAGAGCCCATTCATTGGCTTTTTAGATGAAGGGTGATGGGCGCTAACCTGCTGCAGCACCTGGATGCAATTGGGTACATCTCAATGAGTGATGTGGCTATTACAATTTTAAATGGGAACACACATAATACGTTTGAAATTACACCCTTTGAAACTACTTACACTTATGATTAAAAGGTTGTAGTTTCAATTTTTTAACTGTGAAATGTTTTAATTGTGAAGAGTTTTTTAAAATCATTTTAGAGAGCCTATGAGAAAAGCTTCAGCGTATACAATGATGCTTAAGACATATACAC... |
Task1_train_42191 | This variant is present on Chromosome 12. Is the change likely to result in a pathogenic outcome? | Benign | GGTTCCACTTGGTCTCTAGCACCTGATTCTGCTGCTCCAGGAACCGCACCTGGAACCCAAAGGCAGTCATCGCCCAGAGTCCCCATGTTGTTGCCTCTCAAGAGTGGGGAAAGGGCCCCAAAAACCAGAGGCAGCCATCCTGGGGGACTGGGGGTAGGAGAAAACAAGGCTTATCCCGGGGTGGATTCAGCCGAGGGACATGCTCACCTGGATCTCCAAGACAAGAAATAGGACCCGGTCTATATGGAATCAGGAAGAGGGCTTAAGCAATGGTACCATCTGCCTCTGCCTCAGTGAGTTTTCATGAGACAGAGGTAGCT... | GGTTCCACTTGGTCTCTAGCACCTGATTCTGCTGCTCCAGGAACCGCACCTGGAACCCAAAGGCAGTCATCGCCCAGAGTCCCCATGTTGTTGCCTCTCAAGAGTGGGGAAAGGGCCCCAAAAACCAGAGGCAGCCATCCTGGGGGACTGGGGGTAGGAGAAAACAAGGCTTATCCCGGGGTGGATTCAGCCGAGGGACATGCTCACCTGGATCTCCAAGACAAGAAATAGGACCCGGTCTATATGGAATCAGGAAGAGGGCTTAAGCAATGGTACCATCTGCCTCTGCCTCAGTGAGTTTTCATGAGACAGAGGTAGCT... |
Task1_train_42192 | Chromosome 12 carries this variant. Does this mutation lead to a specific disease, or is it non-pathogenic? | Benign | CCAGAGGCAGCCATCCTGGGGGACTGGGGGTAGGAGAAAACAAGGCTTATCCCGGGGTGGATTCAGCCGAGGGACATGCTCACCTGGATCTCCAAGACAAGAAATAGGACCCGGTCTATATGGAATCAGGAAGAGGGCTTAAGCAATGGTACCATCTGCCTCTGCCTCAGTGAGTTTTCATGAGACAGAGGTAGCTTCTCATGCTATAAATGCTGGTGTTTTCTGAGTAAAGAGAAATGGGGAGCAGGGGAGAAACAGGGACTGGGGAGTGACATTGGAAAGCACACTGGCATTTAGAGCGTTCCTCCTGTTGTGTAGCC... | CCAGAGGCAGCCATCCTGGGGGACTGGGGGTAGGAGAAAACAAGGCTTATCCCGGGGTGGATTCAGCCGAGGGACATGCTCACCTGGATCTCCAAGACAAGAAATAGGACCCGGTCTATATGGAATCAGGAAGAGGGCTTAAGCAATGGTACCATCTGCCTCTGCCTCAGTGAGTTTTCATGAGACAGAGGTAGCTTCTCATGCTATAAATGCTGGTGTTTTCTGAGTAAAGAGAAATGGGGAGCAGGGGAGAAACAGGGACTGGGGAGTGACATTGGAAAGCACACTGGCATTTAGAGCGTTCCTCCTGTTGTGTAGCC... |
Task1_train_42193 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | TATTTTTCAAAAGAATTTCCTGATTGTTAAAATTAGGGAGTTTCTGCTGGTCCCACTATAAGAAAGAGACTGCCAAACCCTGTGGGGCCAGCATTAAACTGGCTTGCACAGTGGTCCACACACCAGTCTCCACTCCCATTGAGGAGGCACCACTCTGTGCTCAGTTTCCTTCATGCAGGAGAGCCGGTGTGGGGGTGACAGAAGAGGGGAGGGGCTGAGAGTTTCACCACAGCAGGCAGGAGATTGCTATGAAAGAGGCTAGTGTGCAGTATCAGAATGTCCTGGGCACTAGCTCCACCTGGAAGAAGTAGCTCTGAATG... | TATTTTTCAAAAGAATTTCCTGATTGTTAAAATTAGGGAGTTTCTGCTGGTCCCACTATAAGAAAGAGACTGCCAAACCCTGTGGGGCCAGCATTAAACTGGCTTGCACAGTGGTCCACACACCAGTCTCCACTCCCATTGAGGAGGCACCACTCTGTGCTCAGTTTCCTTCATGCAGGAGAGCCGGTGTGGGGGTGACAGAAGAGGGGAGGGGCTGAGAGTTTCACCACAGCAGGCAGGAGATTGCTATGAAAGAGGCTAGTGTGCAGTATCAGAATGTCCTGGGCACTAGCTCCACCTGGAAGAAGTAGCTCTGAATG... |
Task1_train_42194 | A variant on Chromosome 12 has been observed. Is this a neutral mutation, or does it result in a disease? If so, which one? | Benign | TATTCTTGCAGTTGTTCAGGTCCAGCTGCTGTAGCAGCTCCCACTTGGTCTCCAGCACCTGGTTCTGCTGCTCCAGGAACCGCACCTGGAACCCATGCCACACATACTTAAGCAATGTGGAGAGGGGATGTGAGAATTCCCTTCCTGGACAGGAACTGTGTTTTCTTATGCTACATTAGCTTTAAAAATGAGCCTCAGCCCTTAAAAACTGCCACCCATGCCACTCACACCCCCACTCCTTACCTAGGGTCCTTTATCTGACTGAAGTTCTCACTCTGAGGCAGCCCTTAAGGTTGGGAGGGGCACCAATGTCTTCATTT... | TATTCTTGCAGTTGTTCAGGTCCAGCTGCTGTAGCAGCTCCCACTTGGTCTCCAGCACCTGGTTCTGCTGCTCCAGGAACCGCACCTGGAACCCATGCCACACATACTTAAGCAATGTGGAGAGGGGATGTGAGAATTCCCTTCCTGGACAGGAACTGTGTTTTCTTATGCTACATTAGCTTTAAAAATGAGCCTCAGCCCTTAAAAACTGCCACCCATGCCACTCACACCCCCACTCCTTACCTAGGGTCCTTTATCTGACTGAAGTTCTCACTCTGAGGCAGCCCTTAAGGTTGGGAGGGGCACCAATGTCTTCATTT... |
Task1_train_42195 | A variant on Chromosome 12 is under investigation. Evaluate whether it is clinically benign or pathogenic and name the disorder if relevant. | Benign | GACTAAGCATACACTAGGTGGGATGAAAATCATGTAACCGTCTACTCCTGGGCCTCTCCCAAGGTTGTCCTGAGAATTGTAGTGAGAGGCACCTGTATTTCTGAGCCTCCTAGTTAACATTCAGCACTTAAGCCAGTTATGGTAAGTGCCCCCAGACAGAAGCTTGTCCATGGCAAATACCTTAAATGGACTTCCTGTTTCAGAAATCATCTGTGCACCCTTGGGTTGGGGAGGGGGATAGGAGACAAATGCATTTTGACCTCTGAAGTACAGTAGGCACAGGAATGGGCACAGGGCTTGTCTCTTCCCCAGGGGAAATG... | GACTAAGCATACACTAGGTGGGATGAAAATCATGTAACCGTCTACTCCTGGGCCTCTCCCAAGGTTGTCCTGAGAATTGTAGTGAGAGGCACCTGTATTTCTGAGCCTCCTAGTTAACATTCAGCACTTAAGCCAGTTATGGTAAGTGCCCCCAGACAGAAGCTTGTCCATGGCAAATACCTTAAATGGACTTCCTGTTTCAGAAATCATCTGTGCACCCTTGGGTTGGGGAGGGGGATAGGAGACAAATGCATTTTGACCTCTGAAGTACAGTAGGCACAGGAATGGGCACAGGGCTTGTCTCTTCCCCAGGGGAAATG... |
Task1_train_42196 | This alteration on Chromosome 12 may affect genome function. Does it lead to a disease or is it benign? | Benign | ATAGGGAAGTGCCCGGAACCATCCCAAAATGGAGCCAGGTGGGATTCCAAAAAACAAAGCACTAAACACCAGGGTGATCAGTGTGCAGTATTTAAAAGGAGGACTAAAGGTTCAGAGTGAAGTGCAGCATTCTCACGGTGGACAGGGACATGAGGGATGTTCTAGCTGGGTATGTCTGCAGTTAAGGAGTCAGGTTATGGAATTTCATAGACGAGTTTAAGGAATTTGGCTCAGGGCGAAGGCTAGTTTCTGTGTGTTTAACAAAAGGGCTATTTCCCAGTGTTTCCCAGCAACAACTAAACAGCTTTGTCAGTGCCTGA... | ATAGGGAAGTGCCCGGAACCATCCCAAAATGGAGCCAGGTGGGATTCCAAAAAACAAAGCACTAAACACCAGGGTGATCAGTGTGCAGTATTTAAAAGGAGGACTAAAGGTTCAGAGTGAAGTGCAGCATTCTCACGGTGGACAGGGACATGAGGGATGTTCTAGCTGGGTATGTCTGCAGTTAAGGAGTCAGGTTATGGAATTTCATAGACGAGTTTAAGGAATTTGGCTCAGGGCGAAGGCTAGTTTCTGTGTGTTTAACAAAAGGGCTATTTCCCAGTGTTTCCCAGCAACAACTAAACAGCTTTGTCAGTGCCTGA... |
Task1_train_42197 | With a mutation on Chromosome 12, classify this variant as benign or pathogenic. Include the disease if it's pathogenic. | Benign | CAATGTGGGAAGCCAAGGTGGGAGGATCACCTGAGCCCAGGAGTTCAAGACCAGCCTTGGAAACATGGTGAGACCCCATCTTTATTTAGAAGAAAGAAGAAAAAGAGGAGAAGATGAAGATGAAGATGGAAGAATGAGAAGGAGAAGGAGAAGAAGAAGAAGGAGGAGGAGAGGAGGAGGAGGAAGAGGAGGAGGAGGGAAGAAGAAGAAGAGGAGGAGGAGGGAGGAGGAGGAGGGAGTAGGGGGAGGAGGAGGGAGGAGGAGGAGGAAGAGGAGGAAGGAGAAGAAGAGGAGGGAGAAGAGGAGGAAGGCAAAGGAGA... | CAATGTGGGAAGCCAAGGTGGGAGGATCACCTGAGCCCAGGAGTTCAAGACCAGCCTTGGAAACATGGTGAGACCCCATCTTTATTTAGAAGAAAGAAGAAAAAGAGGAGAAGATGAAGATGAAGATGGAAGAATGAGAAGGAGAAGGAGAAGAAGAAGAAGGAGGAGGAGAGGAGGAGGAGGAAGAGGAGGAGGAGGGAAGAAGAAGAAGAGGAGGAGGAGGGAGGAGGAGGAGGGAGTAGGGGGAGGAGGAGGGAGGAGGAGGAGGAAGAGGAGGAAGGAGAAGAAGAGGAGGGAGAAGAGGAGGAAGGCAAAGGAGA... |
Task1_train_42198 | A mutation is present on Chromosome 12. Based on this information, is the variant pathogenic or benign? Provide the disease if relevant. | Benign | CCTACCTTGCCAACTCACGCAGCCTCTGCCTCTAACTGGAATGTTTGTGCTCACCCTGGGCTACCGATCTTCCAAAAAGGTGGGAGCAGGAACAGCAGCAGGGCCAGCAGAGCGGGGTCTGAGTGAGAATGTGCCTAGCTGTGAATCTGACTGCAAGCCAGTGCCCTCCAAAGAGAGATCTGCTGTTTGGACTTATCCACCCTGCTTCCCCCATTAGAGTCGAATTTATTGGCAAAATTGCTGAGACCCATTAAGAAAAGTGAATGAGAGGGGATCAGGAAGGGCGTGGAGGGGAGGAGTTTGAGGAGAGGGCGGTGAGG... | CCTACCTTGCCAACTCACGCAGCCTCTGCCTCTAACTGGAATGTTTGTGCTCACCCTGGGCTACCGATCTTCCAAAAAGGTGGGAGCAGGAACAGCAGCAGGGCCAGCAGAGCGGGGTCTGAGTGAGAATGTGCCTAGCTGTGAATCTGACTGCAAGCCAGTGCCCTCCAAAGAGAGATCTGCTGTTTGGACTTATCCACCCTGCTTCCCCCATTAGAGTCGAATTTATTGGCAAAATTGCTGAGACCCATTAAGAAAAGTGAATGAGAGGGGATCAGGAAGGGCGTGGAGGGGAGGAGTTTGAGGAGAGGGCGGTGAGG... |
Task1_train_42199 | A variant was discovered on Chromosome 12. Please indicate if this mutation results in a known disease or if it's non-harmful. | Benign | GACAGTTGGAGACCATTTAATGGTTAAGTTTCCAGAGCTCGATCTGGCAGGGCATTGTAGGAGGTGCAGGGCTTGGTCAGCCCTCCCTAAGCACCCGTCCCACCTGCTTCTTCACGTTGCTGATCTCTGCCTGCAGCCTCTGGACGGTGCGGTTGAGCTCTGCAATCTCCATCTTGCTGTTCTTCAGGTCGTCTCCATGTCTCCCTGCCGTGATCTGGAGCTCCTGGTACTGGGGCCAAAGGCAGCATCATAGTCAGCATGTGCTGCCCACCACAAGCCCCTCCAGGAGGGAGTAGGTCTGGGCTGCTCTCCCCTGGGAG... | GACAGTTGGAGACCATTTAATGGTTAAGTTTCCAGAGCTCGATCTGGCAGGGCATTGTAGGAGGTGCAGGGCTTGGTCAGCCCTCCCTAAGCACCCGTCCCACCTGCTTCTTCACGTTGCTGATCTCTGCCTGCAGCCTCTGGACGGTGCGGTTGAGCTCTGCAATCTCCATCTTGCTGTTCTTCAGGTCGTCTCCATGTCTCCCTGCCGTGATCTGGAGCTCCTGGTACTGGGGCCAAAGGCAGCATCATAGTCAGCATGTGCTGCCCACCACAAGCCCCTCCAGGAGGGAGTAGGTCTGGGCTGCTCTCCCCTGGGAG... |
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